Assoc. for Accessible Medicine v. Brian Frosh
Opinion of the Court
The Association for Accessible Medicines ("AAM") appeals the district court's dismissal of its dormant commerce clause challenge to a Maryland statute prohibiting price gouging in the sale of prescription drugs. AAM also appeals the district court's refusal to enjoin enforcement of the statute on the basis that it is unconstitutionally vague. We hold that the statute violates the dormant commerce clause because it directly regulates the price of transactions that occur outside Maryland.
I.
Factual Background and Procedural History
A.
Maryland's Anti-Price Gouging Statute
In response to reports of price gouging by pharmaceutical manufacturers in the sale of certain prescription medications, Maryland's legislature passed HB 631, "An Act concerning Public Health-Essential Off-Patent or Generic Drugs-Price Gouging-Prohibition" (the "Act"), during the 2017 legislative session. J.A. 42-48.
The Act prohibits "[a] manufacturer or wholesale distributor" from "engag[ing] in price gouging in the sale of an essential off-patent or generic drug."
A manufacturer or wholesale distributor determined to be in violation of the Act may face a number of legal consequences, including a civil penalty of $10,000 per violation or an action to enjoin the sale of the medication at the increased price.
See
B.
AAM's Suit Challenging the Act
AAM is a voluntary organization with a membership that consists of prescription drug manufacturers and wholesale distributors and other entities in the pharmaceutical industry. AAM's member-manufacturers, only one of which is based in Maryland, typically sell their products to wholesale pharmaceutical distributors, none of which are based in Maryland . The vast majority of these sales occur outside Maryland's borders.
On July 6, 2017, AAM filed this action against Brian Frosh, Maryland's Attorney General, and Dennis R. Schrader, Secretary of the Maryland Department of Health (collectively, "Maryland"). Among other claims, AAM asserts that the Act violates the dormant commerce clause and is unconstitutionally vague. Maryland filed a motion to dismiss AAM's suit, which the district court granted as to the dormant commerce clause claim but denied as to the vagueness claim. The district court also denied AAM's motion for a preliminary injunction. AAM timely appealed.
II.
Dormant Commerce Clause Challenge
AAM argues that the district court improperly dismissed its claim that the Act violates the dormant commerce clause by directly regulating wholly out-of-state commerce. We review the dismissal de novo, "accepting [AAM's] well-pleaded allegations as true and drawing all reasonable inferences in [AAM's] favor."
Schilling v. Schmidt Baking Co.
,
A.
The Dormant Commerce Clause and the Principle Against Extraterritoriality
Implicit in the constitutional allocation of the "Power ... To regulate Commerce ... among the several States," U.S. Const. art. I, § 8, cl. 3, to the federal government is a corollary "constraint on the power of the States to enact legislation that interferes with or burdens interstate commerce."
Brown v. Hovatter
,
The principle against extraterritoriality as it relates to the dormant commerce clause is derived from the notion that "a State may not regulate commerce occurring wholly outside of its borders."
Star Sci., Inc. v. Beales
,
1.
One of the earliest cases to address the extraterritoriality principle as it relates to the dormant commerce clause is
Baldwin v. G.A.F. Seelig, Inc.
,
A plurality of the Court expounded on this concept nearly half a century later in
Edgar v. MITE Corp.
,
The Court favorably referenced both
Baldwin
and
Edgar
in
Brown-Forman Distillers Corp. v. New York State Liquor Authority
,
Just three years later, the Supreme Court considered a similar Connecticut law in
Healy v. Beer Institute
,
1) A state statute may not regulate "commerce that takes place wholly outside of the State's borders, whether or not the commerce has effects within the State." Id. at 336,109 S.Ct. 2491 . Specifically, a state law may not have "the practical effect of establishing 'a scale of prices for use in other states.' "Id. (quoting Baldwin ,294 U.S. at 528 ,55 S.Ct. 497 ).
2) "A statute that directly controls commerce occurring wholly outside the [legislating state's] boundaries ... is invalid regardless of whether the statute's extraterritorial reach was intended by the legislature."Id. The statute's "practical effect" is the focus of the inquiry.Id.
3) In evaluating a statute's "practical effect," the Court considers "not only ... the consequences of the statute itself, but also ... how the challenged statute may interact with the legitimate regulatory regimes of other States and what effect would arise if ... every[ ] State adopted similar legislation." Id. at 336,109 S.Ct. 2491 . This is because "the Commerce Clause protects against inconsistent legislation arising from the projection of one state regulatory regime into the jurisdiction of another State."Id. at 336-37 ,109 S.Ct. 2491 .
Applying these three directives, the Court invalidated the Connecticut law due to its "undeniable effect of controlling commercial activity occurring wholly outside the boundary of the State."
2.
Maryland asserts that in
Pharmaceutical Research & Manufacturers of America v. Walsh
,
Maryland's reading of this language, while adopted by two of our sister circuits, is too narrow. The Supreme Court's statement does not suggest that "[t]he rule that was applied in
Baldwin
and
Healy
" applies
exclusively
to "price control or price affirmation statutes."
See
Walsh
,
B.
AAM's Challenge to the Act
We now turn to the merits of AAM's dormant commerce clause challenge. AAM asserts that the Act directly regulates the prices charged for prescription drugs in out-of-state transactions, even though its provisions are triggered only when one of those drugs is available for sale in Maryland. Maryland acknowledges that the Act is intended to reach the manufacturers' conduct in the series of wholesale transactions that occur "upstream" from consumer retail sales but argues that these indirect effects do not violate the dormant commerce clause's prohibition on direct regulation.
We agree with AAM that the district court erroneously upheld the Act under the dormant commerce clause. First, the Act is not triggered by any conduct that takes place within Maryland. Second, even if it were, the Act controls the prices of transactions that occur outside the state. Finally, the Act, if similarly enacted by other states, would impose a significant burden on interstate commerce involving prescription drugs. All of these factors combine to create a violation of the dormant commerce clause.
1.
The Act is Not Limited to Sales Wholly Within Maryland
In reaching its conclusion, the district court emphasized that the Act's provisions "are triggered only when there is a drug ... made available for sale
within
the state." J.A. 486 (emphasis in original). The district court likened the Act to the Virginia statute at issue in
Star Scientific
, but this comparison is inapposite.
See
id.
at 485-86. The Virginia statute at issue in
Star Scientific
did not apply to sales to distributors, retail chains, or consumers
outside Virginia
. Instead, it specifically required tobacco manufacturers selling cigarettes
in Virginia
to join a nationwide settlement agreement or place into escrow a fee of two cents per cigarette actually sold in the state.
See
Star Sci.
,
In contrast, here, the Act's plain language allows Maryland to enforce the Act against parties to a transaction that did not result in a single pill being shipped to Maryland. Specifically, the Act prohibits "price gouging in the sale of an essential off-patent or generic drug."
Therefore, the Act targets conduct that occurs entirely outside Maryland's borders, a conclusion supported by the Act's prohibition of a manufacturer's use of the defense that it did not directly sell to a consumer in Maryland.
See
2.
The Act Impacts Transactions that Occur Wholly Outside Maryland
Even if the Act did require a nexus to an actual sale in Maryland, it is nonetheless invalid because it still controls the price of transactions that occur wholly outside the state.
See
Brown-Forman
,
Therefore, the Act effectively seeks to compel manufacturers and wholesalers to act in accordance with Maryland law outside of Maryland. This it cannot do.
See
Healy
,
More importantly, the Act is effectively a price control statute that instructs manufacturers and wholesale distributors as to the prices they are permitted to charge in transactions that do not take place in Maryland. This is precisely the conduct "[t]he rule that was applied in
Baldwin
and
Healy
" aims to prevent.
Walsh
,
3.
The Act Implicates a Price Control as Opposed to an Upstream Pricing Impact
Maryland attempts to justify the Act by arguing that its out-of-state pricing implications are merely "the upstream pricing impact of a state regulation."
Freedom Holdings, Inc. v. Spitzer
,
Therefore, the fundamental problem with the Act is that it "regulate[s] the price of [an] out-of-state transaction."
Walsh
,
4.
The Act Burdens Interstate Commerce in Prescription Drugs
The Act's significant scope is further illuminated by the burden similar legislation would place on interstate commerce.
See
Healy
,
In upholding the Act, the district court referred to this conundrum as a "practical problem" and suggested that prescription drug manufacturers could simply modify their distribution systems to track the shipments of drugs bound for Maryland and isolate those drugs in order to comply with the Act. J.A. 489-90. It is indeed true that the dormant commerce clause does not "protect[ ] the particular structure or methods of operation in a retail market."
Exxon Corp. v. Governor of Md.
,
5.
In sum, we hold that the Act is unconstitutional under the dormant commerce clause because it directly regulates transactions that take place outside Maryland . We therefore reverse the district court's dismissal of this claim and remand this matter to the district court with instructions to enter judgment in favor of AAM.
To be clear, we in no way mean to suggest that Maryland and other states cannot enact legislation meant to secure lower prescription drug prices for their citizens. Indeed, the Supreme Court upheld a Maine law with that very aim in
Walsh
.
See
Although we sympathize with the consumers affected by the prescription drug manufacturers' conduct and with Maryland's efforts to curtail prescription drug price gouging, we are constrained to apply the dormant commerce clause to the Act. Our dissenting colleague suggests that by doing so, we imply that prescription drug manufacturers have a constitutional right to engage in price gouging. See post at 692-93. This is a sweeping and incorrect conclusion to draw from our holding that Maryland is prohibited from combating prescription drug price gouging in the manner utilized by the Act . Prescription drug manufacturers are by no means "constitutionally entitled," id. at 57, to engage in abusive prescription drug pricing practices. But Maryland must address this concern via a statute that complies with the dormant commerce clause of the U.S. Constitution.
III.
Conclusion
For the foregoing reasons, we reverse the district court's dismissal of AAM's dormant commerce clause challenge and remand with instructions to enter judgment in favor of AAM. AAM's request for an injunction pending this appeal is denied as moot.
REVERSED AND REMANDED WITH INSTRUCTIONS
Because we hold that the statute is unconstitutional pursuant to the dormant commerce clause, we need not address whether it is also void for vagueness.
Citations to the "J.A." refer to the Joint Appendix filed by the parties in this appeal.
Thus, even if we applied a limiting construction to require a consumer sale in Maryland prior to enforcement of the Act, Maryland's own interpretation of the Act clarifies that it targets not a consumer retail sale but the manufacturer's initial sale of the drug.
AAM challenges the Act only as it applies to these out-of-state sales.
Dissenting Opinion
After a series of high-profile incidents in which several generic pharmaceutical manufacturers imposed multiple-thousand-fold price increases for single-source generic drugs that treat rare and life-threatening conditions, the Maryland legislature enacted legislation prohibiting "unconscionable" price increases for certain generic drugs "made available for sale" to Maryland consumers. Md. Code Ann. Health-Gen. §§ 2-801 to - 803 (2017). But a trade association representing generic pharmaceutical manufacturers-which styles itself the "Association for Accessible Medicines" ("AAM" or "Plaintiff")-brought this action to enjoin the Maryland statute on grounds that it violates the dormant Commerce Clause and is unconstitutionally vague. The district court upheld Maryland's authority under the dormant Commerce Clause to protect its citizens from the abusive pricing practices at issue. I agree with the district court's holding, but my colleagues in the majority hold otherwise.
In particular, the majority opinion holds that the Maryland statute violates the dormant Commerce Clause's "extraterritoriality doctrine" to the extent that it applies to sales of generic drugs between manufacturers and distributors consummated outside of Maryland, even when the generic drugs involved in such out-of-state transactions are subsequently resold to Maryland consumers. Ante at 671-72. Put differently, the majority opinion concludes that the Commerce Clause bars Maryland from protecting its citizens against unconscionable pricing practices by out-of-state generic drug manufacturers who distribute their drugs to Maryland's citizens through an out-of-state intermediary. That conclusion conflicts with the approach taken by several of our sister circuits in deciding whether a state statute's extraterritorial reach violates the dormant Commerce Clause.
Contrary to the majority opinion's conclusion, Maryland is authorized under its "general police powers to regulate matters of legitimate local concern."
Lewis v. BT Inv. Mgrs., Inc.
,
I.
Two recent reports by the federal government regarding generic drug pricing gave rise to Maryland taking action to protect its citizens from abusive pricing practices by a subset of generic drug manufacturers. Both reports were prompted by media stories highlighting significant increases in the price of certain generic drugs. See, e.g. , Jonathan D. Alpern et al. , High-Cost Generic Drugs-Implications for Patients and Policy Makers, 371 N. Engl. J. Med. 1859, 1859-60 (2014); Andrew Pollack, Once a Neglected Treatment, Now an Expensive Specialty Drug , N.Y. Times, Sept. 21, 2015, at B1.
The first report, prepared by the Government Accountability Office ("GAO") in response to a request by a bipartisan group of legislators, examined pricing trends for generic drugs covered by the Medicare program's outpatient prescription drug benefit, commonly referred to as "Medicare Part D." See U.S. Gov't Accountability Off., GAO-16-706, Generic Drugs Under Medicare: Part D Generic Drug Prices Declined Overall, but Some Had Extraordinary Price Increases (2016) [hereinafter, "GAO Report"]. The GAO Report found that for a basket of 1,441 "established generic drugs"-"drugs that were continuously billed under Medicare Part D ... during [the] study period"-prices fell, on average, 0.7 percent per quarter from the first quarter of 2010 through the second quarter of 2015. See id. at 9. Although prices for established generic drugs generally declined during the 2010 to 2015 period, the GAO Report further found that "315 of the 1,441 established drugs experienced an extraordinary price increase-a price increase of at least 100 percent." Id. at 12. Notably, the number of established drugs experiencing a price increase of at least 100 percent increased during the five-year study period:
45 drugs experienced such an increase between the first quarter of 2010 and the first quarter of 2011, whereas 103 drugs experienced such an increase between the first quarter of 2014 and the first quarter of 2015. Id. at 12, 18.
A smaller subset of established generic drugs experienced even more "extraordinary" price increases-48 such drugs experienced a price increase of 500 percent or greater and 15 such drugs experienced a price increase of 1,000 percent or greater. Id. at 14. The vast majority of these extraordinary price increases persisted throughout the term of the study. Id. at 18.
Most of the established generic drugs experiencing extraordinary price increases were not among the 100 most heavily prescribed established generic drugs covered under Medicare Part D. To that end, stakeholders interviewed by GAO reported that "[i]f a generic drug serves a small [patient] population, ... it [is] more susceptible to price increases" because "there may be little financial incentive for a [competing] manufacturer to enter the market" and thus less "downward pressure on price." Id. at 24. Stakeholders also reported that supplier and buyer consolidation can drive price increases, as can difficulty manufacturing a particular generic drug. Id.
The second report, prepared by the United States Senate Special Committee on Aging, investigated and analyzed several "abrupt and dramatic" price increases for certain generic drugs.
See
Senate Special Comm. on Aging,
Sudden Price Spikes in Off-Patent Prescription Drugs: The Monopoly Business Model that Harms Patients, Taxpayers, and the U.S. Health Care System
3 (2016) [hereinafter, "Senate Report"]. The Senate Report examined the circumstances surrounding large price increases for seven generic drugs, all of which had lacked patent protection for decades, sold by four generic pharmaceutical companies-two of which were formed and managed by since-convicted investor Martin Shkreli.
The Senate investigation revealed that the four companies followed a common "business model" in acquiring and marketing the seven generic drugs. Id. at 4. In particular, each case involved a (1) single-source generic drug (2) distributed through a "closed distribution system" that (3) was essential to-the "gold standard" for-(4) treating a rare condition. Id. at 4, 30-31. Each of these four characteristics allowed the company to "exercise de facto monopoly pricing power, and then impose and protect astronomical price increases," the Senate committee found. Id. at 4.
For example, single-source drugs distributed through closed-distribution systems-which make it harder for potential entrants to bring to market a competitive product or attract and retain patients-are unlikely to face competition, thereby allowing sellers to charge monopoly prices, notwithstanding the generic drug's lack of patent protection. Id. at 4, 30-31. Likewise, when a generic drug is the "gold standard" for treating a particular condition, physicians continue to prescribe the drug, even in the face of substantial price increases. Id. at 30; see also , e.g. , id. at 56 (chief executive of one generic firm explaining that it had monopoly "pricing power" for a generic drug that is the standard-of-care for treating a rare and deadly disease because, absent the drug, patients would face "liver failure or a liver transplant or even death"). And because the generic drugs treat a "rare" condition "the patient population dependent upon them [is] too small to organize effective opposition to the price increase." Id. at 31.
The Senate Report found that the large price increases "devastated patients ... across the nation," many of whom were "forced to go without vital medicine[s]" or switch to alternative, potentially less effective, therapies. Id. at 7-8. The price increases also harmed providers. For example, the Johns Hopkins Health System, which is headquartered in Maryland, reported that it lost nearly $1 million in 2015 alone as a result of several-hundred-fold price increases for two of the drugs. Id. at 6-8. The price increases also led to increases in spending by governmental health care programs, including state Medicaid programs. Id. at 110. The report further concluded that existing federal competition laws were inadequate to prevent the dramatic price increases and suggested several statutory and regulatory remedies. Id. at 116-25.
After reviewing these reports, the Maryland legislature decided to enact legislation to combat what it concluded were abusive pricing practices by certain generic drug suppliers. To that end, on May 27, 2017, the Maryland General Assembly passed HB 631. That statute, which went into effect on October 1, 2017, prohibits manufacturers and distributors from engaging in "price gouging" in the sale of an "essential off-patent or generic drug." Md. Code Ann. Health-Gen. § 2-802(a). The statute exempts "wholesale distributors" from liability, however, if they impose a price increase that "is directly attributable to additional costs for the drug imposed on the wholesale distributor by the manufacturer of the drug." Id. § 2-802(b).
HB 631 defines "essential off-patent or generic drug" as a drug: (1) "[f]or which all exclusive marketing rights, if any, granted under the federal Food, Drug, and Cosmetic Act, § 351 of the federal Public Health Service Act, and federal patent law have expired"; (2) that is listed on the Model List of Essential Medicines, as adopted by the World Health Organization, or that has been has been designated, according to specified criteria, an "essential medicine" by the Maryland Secretary of Health; (3) "[t]hat is actively manufactured and marketed for sale in the United States by three or fewer manufacturers"; and (4) that is "made available for sale" in the State of Maryland. Id. § 2-801(b)(1). "Essential off-patent or generic drug" also includes any "drug-device combination product used for the delivery of a drug" for which all exclusive marketing rights have expired. Id. § 2-801(b)(2). Although HB 631 regulates only those generic drugs "made available for sale" in Maryland, "a person who is alleged to have violated [the statute] may not assert as a defense that the person did not deal directly with a consumer residing in the State." Id. §§ 2-801(b)(1), 2-803(g).
The statute defines "price gouging" as an "unconscionable increase in the price of a prescription drug." Id. § 2-801(c). Tracking many aspects of the "business model" identified in the Senate Report, the statute provides that an "unconscionable increase" means an increase in price that (1) "[i]s excessive and not justified by the cost of producing the drug or the cost of appropriate expansion of access to the drug to promote public health"; and (2) "[r]esults in consumers for whom the drug has been prescribed having no meaningful choice about whether to purchase the drug at an excessive price" due to the "importance of the drug to their health" and insufficient market competition. Id. § 2-801(f).
HB 631 authorizes the Attorney General to petition a Maryland circuit court to restrain or enjoin violations of the statute; restore money to consumers obtained as a result of violations; require manufacturers that have engaged in "price gouging" to provide the drug to participants in any state health plan or state health program at the drug's last permissible price for a period of up to one year; and order civil penalties of up to $10,000. Id. § 2-803(d).
HB 631 also confers monitoring authority on the State's Medicaid program, the Maryland Medical Assistance Program (the "Medicaid Program"). In particular, the Medicaid Program may notify the Attorney General of certain price increases to an "essential off-patent or generic drug." Specifically, the Medicaid Program may notify the Attorney General if (1) a price increase, either by itself or together with other price increases, would cause a fifty percent or more increase, as measured within a one year time period, to the wholesale acquisition cost or price paid by the Medicaid Program; and (2) it would cost $80 at the wholesale acquisition cost to obtain a thirty day supply of the maximum recommended dosage, a full course of treatment, or if the drug is not made available in such quantities, it would exceed $80 at the wholesale acquisition cost to obtain a thirty day supply or full course of treatment. Id. § 2-803(a). After receiving notification of such an increase, the Attorney General may demand that the manufacturer imposing the increase submit documentation that itemizes the cost of production; provides explanation for the price increase, including information related to any expenditures made to "expand access to the drug," as well as the associated benefits to the public health; and any other relevant information. Id. § 2-803(b).
II.
On appeal, AAM argues that HB 631, as applied to any transaction consummated outside of Maryland's borders, violates the Commerce Clause, regardless of whether the drugs involved in such transaction later are resold in Maryland. Before addressing the merits of that claim, it is first necessary to determine what the Maryland legislature intended when it limited HB 631's extraterritorial reach to generic drugs "made available for sale" in Maryland.
Id.
§ 2-801(b)(1). The district court held, correctly in my view, that HB 631 is "triggered only when there is a drug ... made available for sale
within
[Maryland]."
Ass'n for Accessible Meds. v. Frosh
, No. 17-cv-1860,
To begin, the majority opinion's conclusion that HB 631 requires no "nexus to an actual sale in Maryland,"
id.
at 671, runs contrary to the State's representation as to its own statute's extraterritorial reach. Before the district court and this Court, the State repeatedly asserted that HB 631 "
in no way prohibits
any of AAM's members from selling drugs at a conscience-shocking price to distributors, to the extent that those drugs are later sold in California or in any other state." J.A. 291 (emphasis added);
see also
Appellee's Br. 7 (representing
that HB 631 "applies only when drugs are sold in Maryland"). Put differently, the State represents that HB 631 "does not reach, or purport to reach, any stream of commerce
that does not end in Maryland
." Mem. In Support of Defs.' Mot. to Dismiss, at 23,
Ass'n for Accessible Meds. v. Frosh
, No. 17-cv-1860 (D. Md. Aug. 14, 2017), ECF No. 29-1 (emphasis added). Because pre-enforcement constitutional challenges to state statutes-like AAM's dormant Commerce Clause challenge-are disfavored,
see
Wash. State Grange v. Wash. State Republican Party
,
The majority opinion's conclusion that the statute extends to drugs not ultimately sold in Maryland also conflicts with AAM's understanding of the statute's extraterritorial reach. In particular, AAM asserts that HB 631 "reach[es] 'sale[s]' that take place outside of Maryland,
so long as the objects of those sales are later resold in Maryland
." Appellant's Br. 28 (emphasis added). AAM, therefore, has not challenged the State's representation-and the district court's conclusion-that HB 631 is "triggered only when there is a drug ... made available for sale
within
[Maryland]."
Frosh
,
Even if the parties disagreed as to whether the statute's applicability requires an in-state sale, Maryland rules of statutory construction-which this Court must follow-support rejecting the majority opinion's broad interpretation of the statute's extraterritorial reach.
See
Carolina Trucks & Equip., Inc. v. Volvo Trucks of N. Am., Inc.
,
In
Carolina Trucks
, this Court considered a dormant Commerce Clause challenge to a South Carolina statute that prohibited motor vehicle manufacturers from "sell[ing], directly or indirectly, a motor vehicle to a consumer in this State, except through a new motor vehicle dealer."
Like the statute at issue in
Carolina Trucks
, Section 2-801(b)(1)'s limitation of HB 631's reach to essential generic drugs "made available for sale" in Maryland is at least ambiguous as to the statute's extraterritorial reach. In particular, this Court reasonably could interpret the statute as
applying only to those specific unconscionably priced pills that are sold or resold in Maryland-as the State represents and the district court concluded-or as extending to any unconscionably priced generic drug, some pills of which are "made available for sale" in Maryland, regardless of whether the particular pills subject to an enforcement action actually are sold or resold in Maryland-as the majority concludes. And like South Carolina law, Maryland law dictates that "unless an intent to the contrary is
expressly
stated, acts of the legislature will be presumed not to have any extraterritorial effect."
Chairman of Bd. of Trs. of Emps.' Ret. Sys. v. Waldron
,
Additionally, the majority opinion's broad construction of the statute's extraterritorial reach conflicts with the rule of construction, applied by Maryland courts, requiring a court "whenever reasonably possible, [to] construe and apply a statute to avoid casting serious doubt upon its constitutionality."
R.A. Ponte Architects, Ltd. v. Invs.' Alert, Inc
.,
III.
Because HB 631 regulates, at most, sales of essential generic drugs in streams of commerce that end in Maryland, AAM's Commerce Clause challenge is without merit.
The Commerce Clause entrusts Congress with the authority "[t]o regulate Commerce with foreign Nations, and among the several States, and with the Indian Tribes." U.S. Const. art. I, § 8, cl. 3. The Supreme Court "has long recognized that this affirmative grant of authority to Congress also encompasses an implicit or 'dormant' limitation on the authority of the States to enact legislation affecting interstate commerce."
Healy v. Beer Inst.
,
AAM does not argue that HB 631 implicates either of these concerns underlying the Supreme Court's modern dormant Commerce Cause jurisprudence: discrimination against interstate commerce or favoring in-state economic interests over out-of-state economic interests. Rather, AAM contends-and the majority opinion agrees-that HB 631 violates the "extraterritoriality doctrine."
The extraterritoriality doctrine-a judge-made doctrine which states that a State may not regulate "commerce occurring wholly outside [its] boundaries,"
Healy
,
Not only have courts questioned the extraterritoriality doctrine's continuing vitality, judges and commentators also have questioned the constitutional rationale underlying the doctrine, in light of new and expanded modes of interstate commerce, changes to the Supreme Court's interpretation of the Commerce Clause, and the availability of potentially more appropriate constitutional provisions, like the Due Process Clause, to ensure that States do not unduly extend their regulatory authority beyond their borders.
See
Am. Beverage
,
The majority opinion concludes that HB 631 regulates "
commerce
occurring wholly outside the boundaries of [Maryland],"
Healy
,
The Supreme Court first defined "commerce," as that term is used in the Commerce Clause, in
Gibbons v. Ogden
, 22 U.S. (9 Wheat.) 1,
Notwithstanding Chief Justice Marshall's expansive definition of commerce in
Gibbons
, between the late Nineteenth Century and the New Deal the Supreme Court narrowly interpreted the term, treating each distinct transaction within a single stream of economic activity as a piece of "commerce." For example, in
Carter v. Carter Coal Co.
,
The Supreme Court abandoned the production-commerce distinction in a series of cases beginning with
NLRB v. Jones & Laughlin Steel Corp.
,
The now-abandoned production-commerce distinction reflected an effort by the Supreme Court to draw a bright line between the regulatory powers of the States and those of the federal government, each of which the Court viewed as "exclusive."
E.C. Knight
,
Therefore, under the modern definition of "commerce"-which encompasses a stream of transactions-a State regulates "commerce occurring wholly outside of [its borders],"
Healy
,
That is precisely the conclusion the Seventh Circuit reached in
Brand Name Prescription Drugs
. There, a group of pharmacies alleged that certain prescription drug manufacturers were engaged in a price-fixing conspiracy.
In accordance with the meaning of "commerce" adopted in
Jones & Laughlin
and
Wickard
and applied in
Brand Name Prescription Drugs
, none of the three dormant Commerce Clause cases upon which the majority opinion relies-
Baldwin
,
Healy
, and
Brown-Forman Distillers v. N.Y. State Liquor Auth.
,
In
Baldwin
, the Supreme Court considered a New York statute setting minimum prices that New York distributors of milk had to pay to New York dairies.
Milk Control Bd. of Pa. v. Eisenberg Farm Prods.
,
Likewise, in
Brown-Forman
, the Court struck down a New York "price-affirmation" statute that "requir[ed] every liquor distiller or producer that sells liquor to wholesalers within [New York] to sell at a price that is no higher than the lowest price the distiller charges wholesalers anywhere else in the United States."
Healy
also involved a "price-affirmation" statute, pursuant to which Connecticut "require[d] out-of-state shippers of beer to affirm that their posted prices for products sold to Connecticut wholesalers are, as of the moment of the posting, no higher than the prices at which those products are sold in ... bordering states."
Additionally, the Connecticut statute "discriminate[d] against brewers and shippers of beer engaged in interstate commerce" because such brewers faced greater restraints on their pricing than brewers that operated solely within Connecticut.
As then-Judge, now-Justice Gorsuch explained after closely analyzing the Court's opinions in
Baldwin
,
Brown-Forman
, and
Healy
, "[i]n all three cases, then, the Court ... faced (1) a price control or price affirmation regulation, (2) linking in-state prices to those charged elsewhere, with (3) the effect of raising costs for out-of-state consumers or rival businesses."
EELI
,
Other circuits also have recognized the limited scope of the extraterritoriality doctrine, as the Supreme Court applied that doctrine in
Baldwin
,
Brown-Forman
, and
Healy
.
See
Ass'n des Eleveurs de Canards et d'Oies du Quebec v. Harris
,
Here, HB 631 is not a price affirmation statute, nor does it link in-state prices to out-of-state prices. HB 631 also does not dictate the prices that manufacturers or distributors charge to downstream purchasers in States other than Maryland. Additionally, it is undisputed that HB 631 does not favor in-state interests at the expense of out-of-state interests-it subjects out-of-state and in-state manufacturers and distributors to the same unconscionability limitation. And it is undisputed that HB 631 does not discriminate against interstate commerce-manufacturers and distributors remain free to engage in interstate commerce, they just may not charge unconscionable prices for essential generic drugs later sold to Maryland consumers. HB 631, therefore, does not violate the extraterritoriality doctrine, as that doctrine was applied in
Baldwin
,
Brown-Forman
, and
Healy
. Indeed,
Brown-Forman
expressly recognized that "a State may seek lower prices for its consumers"-precisely what HB 631 does-without violating the Commerce Clause.
This Court reached a similar conclusion in
Star Scientific
, which involved a Virginia statute that imposed a per-cigarette escrow obligation on manufacturers of cigarettes sold in Virginia.
Like the statute in Star Scientific , HB 631 applies only to essential generics drugs sold in Maryland. See supra Part II. And like the statute in Star Scientific , HB 631 is not "aim[ed]" at "commerce" outside of Maryland, has no effect on transactions undertaken by out-of-state distributors with consumers outside of Maryland, and does not insist on "price parity" with essential generic drugs sold outside of Maryland. Id. Accordingly, HB 631 implicates none of the extraterritoriality concerns this Court recognized in Star Scientific .
In striking down HB 631, therefore, the majority opinion extends the extraterritoriality doctrine beyond the contexts in which the Supreme Court and this Court previously have applied it. The majority opinion acknowledges that in doing so, it diverges from the approach taken by several of our sister circuits, which interpret the extraterritoriality doctrine far more narrowly. Ante at 669. For several reasons, I do not believe such an expansion is warranted.
To begin, the majority opinion's expansive interpretation of the extraterritoriality doctrine substantially intrudes on the States' reserved powers to legislate to protect the health, safety, and welfare of their citizens.
See, e.g.
,
L'Hote v. City of New Orleans
,
Additionally, the majority opinion's broad construction of the extraterritoriality doctrine also calls into question the constitutionality of numerous state antitrust and consumer protection statutes. For example, many States allow indirect purchasers to seek relief under their state antitrust laws against manufacturers which engage in an antitrust conspiracy, notwithstanding that such indirect purchasers did not purchase the allegedly price-fixed product directly from the manufacturer.
See
California v. ARC Am. Corp.
,
Likewise, numerous States impose safety, quality, and labeling restrictions on goods sold by out-of-state manufacturers through out-of-state distributors to in-state consumers. Courts consistently uphold such statutes in the face of Commerce Clause challenges as legitimate exercises of such States' police powers.
See, e.g.
,
RockyMountain Farmers Union v. Corey
,
* * * * *
In sum, the Supreme Court's Commerce Clause jurisprudence does not support equating a single out-of-state transaction with "commerce" for purposes of the extraterritoriality doctrine. And contrary to the majority opinion's holding, neither the Supreme Court nor this Court ever has relied on the extraterritoriality doctrine as the sole basis to invalidate a state statute regulating products ultimately sold within the state's borders. The majority opinion's application of the extraterritoriality doctrine also conflicts with the approach taken by several of our sister circuits, including in factually indistinguishable cases. And the majority opinion's expansion of the extraterritoriality doctrine significantly incurs on the States' reserved police powers and would render numerous longstanding state laws unconstitutional. In such circumstances, I cannot join the majority opinion's conclusion that HB 631 violates the extraterritoriality doctrine.
IV.
The majority opinion concludes that HB 631 violates the dormant Commerce Clause for two additional reasons: (1) "an analogous restriction imposed by a state other than Maryland has the potential to subject prescription drug manufacturers to conflicting state requirements" and (2) it "interferes with the natural function of the interstate market by superseding market forces that the dictate the price of a good." Ante at 673-74. I conclude that neither argument warrants barring Maryland-or any other State-from protecting its citizens from the abusive generic drug pricing practices the legislature sought to address.
Regarding the first reason,
Healy
directed courts confronted with extraterritoriality challenges to consider "how the challenged statute may interact with the legitimate regulatory regimes of other States and what effect if not one, but many or every, State adopted similar legislation."
As a matter of fact, HB 631 does not "compel[ ] manufacturers to sell prescription drugs ...
at a particular price
."
As a matter of law, the majority opinion does not cite any authority-nor have I found any-holding that the dormant Commerce Clause entitles manufacturers to consummate all sales to a distributor in "a single transaction." On the contrary, as the majority opinion acknowledges,
ante
at 673, courts have recognized that a State can adopt a consumer protection law that may require a manufacturer to sell different products or versions of products for resale in the State than it sells in other States. For example, in
Sorrell
, the Second Circuit considered an extraterritoriality challenge to a Vermont statute that required special labeling on all mercury-containing light bulbs sold in Vermont.
Likewise, in
International Dairy
, the Sixth Circuit considered an extraterritoriality challenge by milk processors to an Ohio law regulating milk products on grounds that "due to the complex national distribution channels through which milk products are delivered" and the costs associated with altering the nationwide distribution system, milk processors would be "forced" to comply with the Ohio law "nationwide."
Like the statutes at issue in
Sorrell
and
International Dairy
, HB 631 does not require generic drug manufacturers to sell drugs destined for resale outside of Maryland at conscionable prices. On the contrary, HB 631 does not purport to regulate the price of essential generic drugs that do not enter Maryland's borders, nor does it bar other States from regulating differently the price of essential generic drugs sold to consumers within their borders. And AAM has not argued-much less proven-that its members could not restructure their distribution processes and contracts to ensure that distributors do not resell unconscionably priced generic drugs into Maryland. Again to the contrary, there would seem to be no obstacle to a generic drug manufacturer entering into a single contract with a distributor for an essential generic drug, under which the manufacturer imposes a conscience-shocking price increase for those pills the distributor resells outside of Maryland and a non-conscience-shocking price increase for the pills the distributor resells in Maryland. The contract could further require the distributor to indemnify the manufacturer against any
liability resulting from any unconscionably priced pills that make their way into the Maryland market, unintentionally or otherwise. Accordingly, "[t]o the extent [HB 631] may be said to 'require' [conscionable pricing for drugs] sold outside [Maryland], then, it is only because the manufacturers are unwilling to modify their production and distribution systems to differentiate between [Maryland]-bound and non-[Maryland]-bound [drugs]."
Sorrell
,
The majority opinion's assertion that HB 631 violates the dormant Commerce Clause because it " 'interferes with the natural function of the interstate market' by superseding market forces that dictate the price of a good" fares no better.
Ante
at 673 (quoting
McBurney v. Young
,
The Senate Report reveals that the generic manufacturers recognized and sought to exploit this bargaining inequality by imposing dramatic price increases. For example, Retrophin CEO Shkreli stated in an email explaining a 1,900 percent increase for one generic drug, which was the "only treatment for a rare disease called cystinuria," that "[t]he next generation of pharma guys (or the smart ones) understand the inelasticity of certain products. The insurers really don't care. They just pass [the price increase] through [to patients]." Id. at 41, 44-45. Likewise, Valeant CEO J. Michael Pearson explained that Valeant had monopoly "pricing power" for another generic drug that is the standard-of-care for treating a rare and deadly disease-and therefore was able to impose a multiple-thousand-fold price increase-because, absent the drug, patients would face "liver failure or a liver transplant or even death." Id. at 6, 56.
By analogy to the issue in this case, the Supreme Court long has recognized that States may "supersede market forces,"
ante
at 673, by imposing wage and price restrictions when gross inequality in bargaining power leads to market failure,
see, e.g.
,
W. Coast Hotel Co. v. Parrish
,
As a matter of law, since the demise of the
Lochner
doctrine, the Supreme Court has held that "[t]he Constitution does not guarantee the unrestricted privilege to engage in a business or conduct it as one pleases," and therefore that "statutes prescribing the terms upon which those conducting certain businesses may contract, or imposing terms if they do enter into agreements, are within the state's competency."
Nebbia v. New York
,
V.
In striking down HB 631-legislation enacted to restrain abusive generic drug pricing practices specifically designed to prey on the special vulnerabilities of a defenseless group of Maryland citizens-the majority opinion "empower[s] the judiciary and leave[s] ... state legislatures and everyone else on the sidelines."
Kolbe v. Hogan
,
At the end of the day, AAM argues-and the majority opinion concludes-that, absent federal regulation, its members are
constitutionally entitled
to impose conscience-shocking price increases on Maryland consumers, so long as AAM's members sell their essential generic drugs to Maryland consumers through out-of-state intermediaries. But "[t]he Constitution does not secure to any one liberty to conduct his business in such fashion as to inflict injury upon the public at large, or upon any substantial group of the people."
Nebbia
,
On March 9, 2018, the U.S. District Court for the Southern District of New York sentenced Shkreli to seven years' imprisonment for securities fraud and conspiracy to commit securities fraud. Stephanie Clifford, Citing "Multitude of Lies," Judge Sentences Shkreli to 7 Years in Fraud Case , N.Y. Times, Mar. 10, 2018, at B2.
The majority opinion notes that in
Pharmaceutical Research & Manufacturers of America v. Walsh
,
The majority opinion also relies on the Supreme Court's decision in
Edgar v. MITE Corp.
,
The majority opinion further maintains that complying with HB 631 "would require more than modification of [manufacturers'] distribution systems; it would force them to enter into a separate transaction for each state in order to tailor their conduct so as not to violate any state's price restrictions." Ante at 673-74. But at this preliminary juncture of the litigation, AAM has put forward no evidence that other States intend to impose similar statutes regulating the pricing of generic drugs, let alone evidence that its members would have to enter into "separate transaction[s]" to comply with multiple such laws, rather than by simply modifying their distribution systems and contracts.
Reference
- Full Case Name
- ASSOCIATION FOR ACCESSIBLE MEDICINES, Plaintiff-Appellant, v. Brian E. FROSH, in His Official Capacity as Attorney General for the State of Maryland; Dennis R. Schrader, in His Official Capacity as Secretary of the Maryland Department of Health, Defendants-Appellees, Chamber of Commerce of the United States of America, Amicus Supporting Appellant, AARP; AARP Foundation; Knowledge Ecology International ; Maryland Citizens' Health Initiative Education Fund, Incorporated; Public Citizen; Public Justice Center; Maryland Citizens' Health Initiative Education Fund, Incorporated; Disability Rights Maryland, Amici Supporting Appellee.
- Cited By
- 24 cases
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- Published