FINDINGS OF FACT AND CONCLUSIONS OF LAW
EAGAN, District Judge.
This matter came on for hearing on October 8-9, 2003, on motion of plaintiff, United States of America, for preliminary injunction against defendants, Rx Depot, Inc., Rx of Canada, LLC, Carl Moore and David Peoples (Dkt.# 2); and motion by defendants for preliminary injunction (Dkt.# 10). Upon consideration of the pleadings and the evidence, the Court finds and concludes as follows:
I.
FINDINGS OF FACT
A.
Procedural History
1. The plaintiff instituted this suit on September 11, 2003, by filing a complaint for injunction (Dkt.# 1) and a motion for a preliminary injunction (Dkt.# 2). Plaintiffs complaint alleged violations by defendants of the Federal Food, Drug, and Cos
metic Act (“FDCA”), 21 U.S.C. §§ 331(d) and (t).
2. Defendants filed a response on October 6, 2003 (Dkt.# 10), wherein they moved for their own preliminary injunction against the plaintiffs attempt to enforce the FDCA. Defendants filed an answer and counterclaim on October 8, 2003 (Dkt.# 14).
3. On October 8-9, 2003, the Court heard and received evidence relating to both preliminary injunction motions. Plaintiff and the defendants presented witnesses and exhibits, and thereafter filed proposed findings of fact and conclusions of law.
B.
The Plaintiff
4. Plaintiff brings this action in its own name pursuant to 21 U.S.C. § 337(a) to preliminarily and permanently enjoin alleged violations of the FDCA by defendants.
C.
The Defendants
5. Defendant Rx Depot, Inc. (“Rx Depot”), was incorporated under the laws of the State of Nevada on December 2, 2002, and does business at 4908 South Memorial Drive, Tulsa, Oklahoma, within the jurisdiction of this Court. Appendix to PI. Memorandum in Support of Plaintiffs Motion for Preliminary Injunction (“App.”) Ex. A, Tab 1. Rx Depot does business throughout the United States.
6. Defendant Rx of Canada, LLC (“Rx Canada”), is a Nevada limited liability company. Rx Canada is owned by defendant Carl Moore’s son, Joe-Max Moore. App. Ex. A, Tab 3.
7. Rx Canada’s website, www.rxofcana-da.net, is substantially similar to Rx Depot’s website, www.rxdepot.com. On the Rx Canada website, links to many purported Rx Canada store locations are actually links to Rx Depot stores, including some stores located in the Northern District of Oklahoma. Similarly, links to some purported Rx Depot locations on the Rx Depot website actually lead to contact information for Rx Canada stores. Transcript of Proceedings, October 8-9, 2003 (“Trans.”) at 66-69; Plaintiffs Preliminary Injunction Hearing Ex. (“Pl.Ex.”) 11-12.
8. Defendant Carl Moore, an individual, is the President of Rx Depot and a member of its Board of Directors. He has overall responsibility for, and authority over, all operations of the corporation, including the sales arrangements involving ordering, purchasing, and shipment of prescription drugs from Canada. He performs these activities at 4908 South Memorial Drive, Tulsa, Oklahoma, within the jurisdiction of this Court. App. Ex. A, Tab 1; Pl.Ex. 6; Trans, at 50,178.
9. Defendant David Peoples, an individual, is the Secretary of Rx Depot. He is responsible for receiving and processing orders for Rx Depot. He performs these activities at 4908 South Memorial Drive, Tulsa, Oklahoma, within the jurisdiction of this Court. App. Ex. A Tab 1; Pl.Ex. 6.
10. Defendants Carl Moore, David Peoples, Rx Depot, and Rx Canada (collectively, “defendants” or “Rx Depot”) operate approximately 85 Rx Depot/Rx Canada stores located throughout the United States, which serve about 800 customers each day. Trans, at 188-89.
D.Operation ofRx Depot/Rx Canada
11. Rx Depot assists individuals in procuring prescription medications from pharmacies in Canada. Trans, at 178-79. Each' Rx Depot/Rx Canada location has one or two employees who accept prescriptions from U.S. customers. Customers also are asked to fill out a medical history form and other forms provided by Rx Depot. Customers can deliver these documents to defendants’ stores in person, or can mail or fax to the nearest Rx Depot/Rx
Canada store. Trans, at 20-24, 44-46, 48, 51-52; Pl.Ex. 2, 6,11-12.
12. Once an Rx Depot/Rx Canada customer has submitted the required forms and prescription to defendants, the papers and the customer’s credit card information or a certified check are transmitted to a cooperating pharmacy in Canada. Trans, at 46, 184, 195. A Canadian doctor rewrites the prescription,
and the Canadian pharmacy fills the prescription, ships the prescription drugs directly to the U.S. customer, and bills the U.S. customer’s credit card. Trans, at 22, 45-46, 48, 51-52; PL Ex. 6.
13. Defendants receive a 10 to 12 percent commission for each sale they facilitate for the Canadian pharmacies. The defendants also receive commissions for refill orders, which generally are arranged directly between customers and the Canadian pharmacies. Trans, at 189-90; Pl.Ex. 6.
14. Defendants are essentially commissioned sales agents for Canadian pharmacies. Trans, at 191.
15. An Oklahoma state court recently ordered the defendants’ stores in Oklahoma to close after finding that the defendants acted as storefronts for Canadian pharmacies and, as such, were operating as unlicensed pharmacies. Trans, at 190-91; PLEx. 25.
16. Defendants admit in their answer to the plaintiffs complaint that they are engaged in the business of causing the shipment of U.S.-manufactured and unapproved, foreign-manufaetured prescription drugs from Canadian pharmacies to U.S. citizens.
See
Defendants’ Answer and Counterclaims, Dkt. # 14, ¶ 6.
17. The defendants actively solicit other individuals to open “affiliate” Rx Depot/Rx Canada stores by distributing promotional materials that describe their business practices and the potential profits to be made from opening a franchise. Defendants estimate that an affiliate would receive an average 9% commission on each sale of Canadian prescription drugs, about $24.75. The net commissions for an affiliate in the first year would be an estimated $141,570, according to the defendants. PI. Ex. 1. The defendants’ affiliate “Agreement” also states, however, that the service “may at some date be determined to be unlawful or otherwise prohibited.”
Id.
at 29.
E.
Prescription Drugs from Foreign Countries
18.Although defendants presented evidence that the amount of prescription drugs shipped from Canadian pharmacies never exceeds a ninety-day supply, Trans, at 184; Pl.Ex. 24, that defendants do not allow Canadian pharmacies to ship temperature-sensitive drugs, Trans, at 193, and that defendants do not deal with any third parties, Trans, at 194, unapproved prescription drugs and drugs imported from foreign countries by someone other than the U.S. manufacturer do not have the same assurance of safety and efficacy as drugs regulated by the Food and Drug Administration (“FDA”). Because the drugs are not subject to FDA oversight and are not continuously under the custody of a U.S. manufacturer or authorized distributor, their quality is less predictable than drugs obtained in the United States. For instance, the drugs may be contaminated, counterfeit, or contain erratic amounts of the active ingredient or different excipients. Also, the drugs may have been held under uncertain storage condi
tions, and therefore be outdated or subpo-tent. Trans, at 127-28, 141-42, 144; App. Ex. B (McGinnis Decl.) at ¶¶ 11,14.
19. Prescription drugs obtained through Rx Depot frequently are dispensed in greater quantities than are requested by the prescribing physician. Although defendants presented evidence that the amount of prescription drugs shipped from Canadian pharmacies never exceeds a ninety-day supply, Trans, at 184; Govt’s Ex. 24, Rx Depot advertises the availability of, and causes the importation of, preset quantities of drugs and dispenses these preset quantities regardless of the quantity of the drug the patient’s U.S. physician prescribed and without directions to take the drug for only the number of days prescribed by the U.S. physician. Trans, at 46-47, 62-63, 97-98; Pl.Ex. 10, 11-12. American patients could, therefore, take a drug for many days more than their physicians intend without supervision. This practice can be dangerous in instances where drugs have potentially life-threatening side effects with continued use. Trans, at 98; App. Ex. C (Katz Decl.) at ¶ 14.
20. Prescription drugs obtained through Rx Depot also do not contain the FDA-approved patient package inserts included with certain prescription drugs in the United States. Nor are prescription drugs obtained through Rx Depot shipped in FDA-approved unit-of-use packaging. This type of packaging is used in the United States to help ensure that certain drugs received by customers arrive in designated dosages with the approved patient package insert. Trans, at 98-104; Pl.Ex. 10, p. 16-17, Ex. 18.
21. The fact that there are currently no known cases of someone being harmed by a drug received as a result of using Rx Depot, Trans, at 137-38, or that plaintiff is currently unaware of anyone being harmed by prescription medications ordered through Rx Depot and imported from Canada, Trans, at 85, does not diminish the legitimate safety concerns of the FDA with unregulated commercial reimportation of U.S.-manufactured drugs by someone other than the manufacturer and importation of foreign-manufactured drugs not approved by the FDA.
F.
Undercover Purchases by FDA
22. In May 2003, FDA made an undercover purchase through Rx Depot. An FDA investigator in Maryland downloaded the necessary Rx Depot order forms and related paperwork from the Rx Depot website and filled them out as though be were a patient. The investigator also prepared a prescription for 60 pills, to be taken twice a day for 30 days, of the FDA-approved prescription drug Serzone, which is used to treat depression. The prescription allowed one refill. On the Rx Depot form, the investigator ordered a 100-pill package offered on the Rx Depot website rather than the 60 pills indicated on the prescription. Trans, at 46-47, 62-63; PI. Ex. 9.
23. On May 10, 2003, a second FDA investigator in Oklahoma took the order forms and prescription to an Rx Depot store located at 5801 N. May, Suite 101, Oklahoma City, Oklahoma. The investigator provided the order forms and prescription to the store manager. The Rx Depot manager accepted the paperwork and faxed or mailed the information to a Canadian pharmacy. The manager did not indicate that ordering a greater number of pills than what the prescription called for would be a problem. In fact, the manager stated that drugs obtained through Rx Depot usually came in packages of 100 pills. Trans, at 43-48; Pl.Ex. 8-9.
24. In late May 2003, FDA received a package from Pharmacy North, Inc., in Winnipeg, Manitoba, Canada. The package contained 99 pills (and was labeled as
containing 100) of a foreign-manufactured version of Serzone, known as APO-Nefa-zodone. The labeling provided with the APO-Nefazodone did not direct the patient to take the drug for 30 days or for any other specified period of time. Trans, at 64-65; Pl.Ex. 10.
25. APO-Nefazodone is not generally recognized among qualified experts as safe and effective for use under the conditions prescribed, recommended, or suggested in its labeling. Trans, at 93; App. Ex. C (Katz Decl.) at ¶¶ 8-11.
26. APO-Nefazodone does not have in effect FDA approval of any new drug or abbreviated new drug applications filed pursuant to 21 U.S.C. §§ 355(b) or (j). It does not have in effect a valid exemption from such approval requirements under 21 U.S.C. § 355(i). Trans, at 94; App. Ex. D (Richman Decl.) at ¶ 4.
27. In the United States, Serzone is sold in “unit-of-use packaging” designed to ensure, as much as possible, that the patient receives a designated dose with an FDA-approved patient package insert. The insert includes important information regarding the drug, such as warnings related to potentially serious side effects. One potential side effect of Serzone, and generic versions of Serzone such as APO-Nefazodone, involves increased risk of serious liver damage. Trans, at 95, 99, 103; Pl.Ex. 17-18.
28. The labeling provided by the Canadian pharmacy with the APO-Nefazodone included fewer and far less descriptive warnings regarding potential side effects than the FDA-approved patient package insert for Serzone. For example, the Canadian instructions do not specify some of the liver failure symptoms listed on the Serzone insert, do not mention drugs that should be avoided when taking APO-Nefa-zodone, and do not convey the sense of urgency reflected in the Serzone insert. These substandard instructions could increase the risk of adverse events, including life-threatening liver failure. Trans, at 95, 101-02,120-21; Pl.Ex. 10,18.
29. Patient safety also can be compromised when a pharmacy provides more pills than the number prescribed by the doctor. In the case of antidepressants such as Serzone and APO-Nefazodone, potential problems associated with taking a longer-than-prescribed course of medication include increased risk for serious liver problems. Pharmacies in the United States typically do not supply patients with refills until their previous prescriptions are nearly completed. Trans, at 97-98, 106.
30. In late July 2003, an FDA investigator made a second undercover purchase by faxing an order for Sporanox to Rx Depot’s Tulsa, Oklahoma, location. Trans, at 20-21; Pl.Ex. 2-3.
31. Sporanox is an FDA-approved prescription drug manufactured in Puerto Rico by Janssen Pharmaceutical, Inc., that is used to treat nail fungal infections. Trans, at 20, 24, 38; Pl.Ex. 5.
32. In early August 2003, FDA received the Sporanox order from Pharmacy North, Inc., in Winnipeg, Manitoba, Canada. The Sporanox was shipped into the United States by a party other than the manufacturer. Trans, at 22-23; Pl.Ex. 4.
33. The drug products purchased by FDA through undercover buys represent just two of the hundreds of prescription drugs advertised on the defendants’ websites. Pl.Ex. 11-12.
34. The fact that the FDA did not test for adulteration the individual tablets of APO-Nefazodone or Sporanox received in the undercover purchases, Trans, at 27-29, 40, 76, or that an American pharmacy would have filled the Sporanox prescription, Trans, at 31, is irrelevant to the safety concerns of the FDA at issue in this case. The safety concerns of the FDA
relate to reimportation of U.S.-manufactured drugs by someone other than the manufacturer and importation of foreign-manufactured drugs not approved by the FDA. Complaint, Dkt. # 1, at ¶¶ 12, 13. Defendant Moore admitted at the hearing that prescription drugs from Canadian pharmacies are not approved by FDA and that some of them are manufactured in the United States. Trans, at 190. Defendants’ websites also state that the advertised drugs are not FDA-approved. Pl.Ex. 11-12.
G.
FDA Warnings to the Defendants
35. On March 21, 2003, FDA issued a Warning Letter to the Rx Depot store located at 200 S. Bloomington, Ste. El, Lowell, Arkansas; copies of the letter were sent to defendants Moore and Peoples. The letter informed the defendants that FDA believed them to be violating 21 U.S.C. § 381(d)(1), because they caused prescription drugs manufactured in the United States to be reimported by persons other than the manufacturer of the drug. Further, the letter stated that the defendants violated 21 U.S.C. § 355 by causing unapproved new drugs to be imported into the United States. Trans, at 69-70, 187-88; Pl.Ex. 13.
36. On May 6, 2003, the defendants responded to FDA’s Warning Letter. Defendants stated that all drugs they cause to be obtained from Canadian pharmacies are “manufactured in the United States.” Defendants also stated that the drugs advertised on Rx Depot’s website and obtained by their customers from Canadian pharmacies “ ‘are not’ FDA approved.” Trans, at 70-71; Pl.Ex. 14.
37. In their response to FDA’s warnings, defendants did not indicate any intention to halt their illegal practices. By letter dated June 10, 2003, FDA informed the defendants that their response was inadequate. Trans, at 71; Pl.Ex. 14-15.
38. Since receiving the FDA Warning Letter, the defendants have opened approximately 50 additional Rx Depot and Rx Canada stores. Trans, at 190.
39. Defendant Moore testified at the hearing that the defendants would continue their activities unless this Court enjoins them. Trans, at 192.
40. FDA has sent numerous other Warning Letters and informational letters to operations similar to Rx Depot and individuals considering engaging in such activities. Pl.Ex. 20. In these letters, some of which pre-date the start of the defendants’ business, FDA has consistently stated to interested parties that “a U.S. pharmacy or other business virtually always violates U.S. law by importing or causing the importation of [drugs from Canadian pharmacies].”
Id.
at 8.
H.
Cost of Prescription Drugs
41. Congress made findings in 2000 regarding the high price of prescription medications in the United States.
See
Medicine Equity and Drug Safety Act of 2000 (the “MEDS Act”), Pub.L. 106-387, § 1(a) [Title VII, § 745(b) ], Oct. 28.2000, 114 Stat. 1549, 1549A-35 (codified as amended at 21 U.S.C §§ 301, 331, 333, 381, 384 (2000)).
42. The United States ranks significantly higher than other countries, including Canada, in terms of prescription drug costs. Trans, at 8, 132-36, 171, 176, and 213.
43. Because of the high cost of prescription drugs in the United States, some citizens cannot afford their medications at U.S. prices. Defendants presented three highly credible witnesses to testify to this effect at the preliminary injunction hearing. These witnesses use or used Rx Depot to purchase their medications at a significantly lower price. Trans, at 38,
162-66, 171-72, and 199-214. The high cost of prescription drugs in the United States especially impacts those on fixed incomes, such as senior citizens and the disabled.
See id.
44. American cities and states are either looking at ways to import drugs from Canada, or are already doing so, to alleviate the high cost of prescription drugs on their citizens. Trans, at 130, 161-70, and 173.
45. Congress has found that “efforts to enable such purchases [of prescription drugs at prices comparable to the prices for such medicines in other countries] should not endanger the gold standard for safety and effectiveness that has been established and maintained in the United States.” MEDS Act, 21 U.S.C.A. § 348, Historical and Statutory Notes, Congressional Finding 5.
46. Not only is Congress the best forum to address the high cost of prescription drugs for U.S. citizens, but also Congress is currently considering legislation which could allow prescription drug importation from Canada.
I.
FDA Personal Use and Enforcement Discretion Policies
47. The FDA has a personal importation policy which allows entry of foreign drugs by U.S. citizens who bring prescription drugs from foreign countries for personal use. Trans, at 128-29; Pl.Ex. 21; Def. Ex. Ip.
48. The FDA also has an “enforcement discretion policy” whereby the FDA allows small quantities of prescription drugs to be brought into the U.S. by individuals for personal use without recourse. Trans, at 130-31. In this regard, the FDA does not enforce the FDCA against individuals who travel to Canada or use the Internet to purchase prescription drugs from Canada for personal use. Trans, at 35-36, 131, 151,163,171, and 175.
49.Any conclusion of law which is more appropriately characterized as a finding of fact is incorporated herein.
II.
CONCLUSIONS OF LAW
1. This Court has jurisdiction over the subject matter and over all parties to this action under 28 U.S.C. §§ 1331, 1337, and 1345, and 21 U.S.C. § 332(a).
2. Venue in this district is proper under 28 U.S.C. §§ 1391(b) and (c).
3. The defendants violate 21 U.S.C. § 331 by causing the importation of prescription drugs from Canadian pharmacies.
4. APO-Nefazodone is one of the prescription drugs that the defendants cause to be imported. It is a drug within the meaning of the FDCA, 21 U.S.C. § 321(g)(1), and a new drug under 21 U.S.C. § 321(p).
5. Defendants violate 21 U.S.C. § 331(d) each time they cause to be introduced or delivered for introduction into interstate commerce unapproved new drugs in violation of 21 U.S.C. § 355. Specifically, the defendants cause the importation of the unapproved new drugs, such as APO-Nefazodone, listed on their website.
6. Sporanox, another one of the prescription drugs the defendants cause to be imported, is manufactured in Puerto Rico. Pursuant to 21 U.S.C. § 321(a)(1), Puerto Rico is a “state” for purposes of 21 U.S.C. § 381(d)(1). Thus, Sporanox is a U.S.manufactured drug and cannot be imported into the United States by anyone other than the drug’s manufacturer.
7. Defendants violate 21 U.S.C. § 331(t) each time they cause the importation of prescription drugs in violation of 21 U.S.C. § 381(d)(1). Specifically, the defendants cause the reimportation of the U.S.manufactured drugs, such as Sporanox, listed on their website. Reimportation of
U.S.-manufactured drugs, even those approved for use in the United States, violates the FDCA, because only the manufacturer of a drug can reimport that drug into the United States. 21 U.S.C. § 381(d)(1).
A.
Preliminary Injunction Standard
8. Plaintiff seeks a preliminary injunction to stop defendants from further FDCA violations. Generally, an injunction may issue where the movant shows: (1) a substantial likelihood of success on the merits; (2) irreparable injury if the injunction is not granted; (3) that injury outweighs any harm the injunction will cause the opposing party; and (4) the injunction is not adverse to the public interest. O
Centro Espirita Beneficiente Uniao Do Vegetal v. Ashcroft,
342 F.3d 1170, 1177 (10th Cir.2003);
SCFC ILC, Inc. v. Visa USA Inc.,
936 F.2d 1096, 1098 (10th Cir.1991). Where an injunction would alter the status quo, a heightened standard of scrutiny normally applies.
O Centro Espirita,
342 F.3d at 1177-78 n. 3.
9. The overriding purpose of the FDCA is to protect the public health.
United States v. Article of Drug ... Bacto-Unidisk,
394 U.S. 784, 798, 89 S.Ct. 1410, 22 L.Ed.2d 726 (1969);
United States v. Undetermined Quantities of Bottles ...,
22 F.3d 235, 238 (10th Cir.1994). It is well settled that where a statute designed to protect the public authorizes injunctive relief, the agency need not prove all of the elements.
See Hecht Co. v. Bowles,
321 U.S. 321, 331, 64 S.Ct. 587, 88 L.Ed. 754 (1944);
United States v. Odessa Union Warehouse Co-op,
833 F.2d 172, 174-75 (9th Cir.1987);
United States v. City of Painesville, Ohio,
644 F.2d 1186, 1193 (6th Cir.1981);
United States v. Diapulse Corp.,
457 F.2d 25, 27-28 (2d Cir.1972). Specifically, where an injunction is authorized by statute, as here, the agency to whom the enforcement of the statute has been entrusted is not required to show irreparable harm.
Mical Communications, Inc. v. Sprint Telemedia, Inc.,
1 F.3d 1031, 1035-36 (10th Cir.1993)(citing
Atchison, Topeka and Santa Fe Railway Co. v. Lennen,
640 F.2d 255, 259 (10th Cir.1981));
Odessa Union,
833 F.2d at 175-76;
Illinois Bell Telephone Co. v. Illinois Commerce Comm’n,
740 F.2d 566, 571 (7th Cir.1984);
Virgin Islands v. V.I. Paving, Inc.,
714 F.2d 283, 286 (3rd Cir.1983);
Environmental Defense Fund, Inc. v. Lamphier,
714 F.2d 331, 338-39 (4th Cir.1983);
Diapulse,
457 F.2d at 28. Violation of such statutes is presumed to cause public harm; the government need only establish that defendants have violated the statute and there exists “some cognizable danger of recurrent violation.”
United States v. W.T. Grant Co.,
345 U.S. 629, 633, 73 S.Ct. 894, 97 L.Ed. 1303 (1953);
Roe v. Cheyenne Mountain Conference Resort, Inc.,
124 F.3d 1221, 1230-31 (10th Cir.1997);
Lennen,
640 F.2d at 260;
Diapulse,
457 F.2d at 28;
United States v. 22 Rectangular & Cylindrical Finished Devices,
714 F.Supp. 1159, 1167 (D.Utah 1989)(“[h]ere, it is sufficient to warrant an injunction under section 332(a) if it is established that the defendants violated section 331 and that such violations likely will continue”).
B.
Status Quo
10. In
O Centro Espirita,
the Court of Appeals rejected an “absolute” approach to defining the status quo, instead holding that “the definition of ‘status quo’ for injunction purposes depends very much on the facts of a particular case.”
O Centro Espirita,
342 F.3d at 1178. The status quo need not be the state of affairs immediately preceding litigation.
Id.
11. Plaintiff contends that, in this case, Congress established the status quo by outlawing the activities in which the defen
dants now engage. Unlike the facts of 0
Centro Espirita
itself, which implicated two seemingly conflicting federal statues, Rx Depot’s importation of prescription drugs clearly violates the law. The decision in
SCFC ILC, Inc. v. Visa USA, Inc.,
936 F.2d 1096 (10th Cir.1991), cited by defendants, is also distinguishable in that it involved a dispute between two private litigants.
Id.
at 1097-98. As set out above, the normal requirements applicable to private litigants do not necessarily apply where, as here, plaintiff seeks to enforce a duly enacted statute designed to protect the public. By definition, such an action can be brought only after the law is broken; where the violation is obvious, preserving the “status quo” as defendants define it would mean protecting illegal activity.
12. Plaintiff has conclusively shown that the relevant statutory provisions explicitly prohibit exactly what the defendants’ continue to do. Weighing the particular facts of this case, as required by
O Centro Espirita,
the Court finds that the defendants altered the status quo when they began to build a nationwide business based on violating the law.
13. Even if plaintiffs motion were construed as an attempt to change the status quo, the relevant preliminary injunction factors as outlined below weigh heavily and eompellingly in plaintiffs favor. Applying the heightened standard in this ease, therefore, would not change the result. O
Centro Espirita
at 1177-78 n. 3.
C.
Preliminary Injunction Factors
14. Regarding the first factor, the defendants openly and notoriously violate the law. As previously noted, the defendants admit the relevant facts. Defendants advertise and handle orders for Canadian pharmacies and are remunerated for their efforts. Their actions encouraging and facilitating the illegal importation of drugs amount to a responsible share in the furtherance of these transactions prohibited by the FDCA. Thus, their actions constitute the requisite “causing” under 21 U.S.C. § 331.
See United States v. Dotterweich,
320 U.S. 277, 284, 64 S.Ct. 134, 88 L.Ed. 48 (1943) (holding liable under FDCA those who have a “responsible share in the furtherance of the transaction which the statute outlaws”);
United States v. Brittain,
931 F.2d 1413, 1419 (10th Cir.1991) (applying the same rationale to the Clean Water Act). Plaintiff has established more than a substantial likelihood that it will succeed on the merits.
15. The evidence conclusively demonstrates that the defendants’ violations will continue absent an injunction by this Court. Defendant Moore admitted that his storefronts would remain open absent a court order. Even aside from this admission, the probability of future violations may be inferred from past unlawful conduct.
Commodity Futures Trading Comm’n v. British American Commodity Options Corp.,
560 F.2d 135, 142 (2d Cir.1977);
see Odessa Union,
833 F.2d at 176.
16. As discussed above, weighing the respective harms to the parties is
not required here; even were such a test necessary, the defendants would suffer only the “harm” of being ordered to refrain from illegal activity. Despite the defendants’ assertions to the contrary, the FDCA is a constitutional exercise of the commerce power.
United States v. Walsh,
331 U.S. 432, 434, 67 S.Ct. 1283, 91 L.Ed. 1585 (1947). The defendants have no vested interest in an illegal business activity.
Diapulse,
457 F.2d at 29 (citations omitted);
see also U.S. v. Articles of Drug,
825 F.2d 1238, 1248 (8th Cir.1987) (a defendant may not successfully defend against the issuance of an injunction by assertions that the injunction would drive it out of business.).
17. As stated above, plaintiff need only show the defendants’ violations of the FDCA in order to prove public harm. “The passage of the statute is, in a sense, an implied finding that violations will harm the public and ought, if necessary, be restrained.”
Diapulse,
457 F.2d at 28 (citing
United States v. City and County of San Francisco,
310 U.S. 16, 60 S.Ct. 749, 84 L.Ed. 1050 (1940));
see Bioganic Safety Brands, Inc. v. Ament,
174 F.Supp.2d 1168, 1179 (D.Colo.2001) (holding in a preemption case that fourth factor is satisfied where Congress has determined the public interest). Here, Congress explicitly found that the unrestricted reimportation of U.S.-manufactured drugs created “an unacceptable risk that counterfeit, adulterated, misbranded, subpotent, or expired drugs will be sold to American consumers.” PL 100-293, Sec. 2 (“Findings”), April 22, 1988 (available on Westlaw at 102 Stat. 95). Defendants’ contention that FDA’s enforcement action would not actually protect the public from anything is not supported by the record and, moreover, irrelevant.
See United States v. Undetermined No. of Unlabeled Cases,
21 F.3d 1026, 1028 (10th Cir.1994) (“The focus of this Court’s inquiry is whether the Act empowered the FDA to take the actions it did and not the efficacy of those actions.”). Once Congress, exercising its delegated powers, has decided the order of priorities in a given area, it is for the courts to enforce them when asked.
TVA v. Hill,
437 U.S. 153, 194, 98 S.Ct. 2279, 57 L.Ed.2d 117 (1978).
18. The Court recognizes that individual customers of the defendants believe that they benefit from the low prescription drug pi'ices offered by Rx Depot/Rx Canada. This Court is not unsympathetic to the predicament faced by individuals who cannot afford their prescription drugs at U.S. prices. However, the defendants are able to offer lower prices only because they facilitate illegal activity determined by Congress to harm the public interest. Congress, not this Court, is the best forum for weighing all of the costs and benefits of the national statutory scheme regulating prescription drug importation.
Cf. United States v. 9/1 Kg. Containers, More or Less, of an Article of Drug for Veterinary Use,
854 F.2d 173, 179 (7th Cir.1988) (“Subjects such as these [FDA approval and certification process] are for Congress and the FDA to consider. Judges’ role is to decipher and enforce the existing scheme, whatever they think of its wisdom.”).
D.
Selective Enforcement Claim
19. Defendants’ claim of unconstitutionally selective enforcement by FDA is unavailing. FDA’s personal importation policy outlines specific circumstances in which the agency generally will decline to prosecute the illegal importation of small quantities of prescription drugs by individuals. By its express terms, this policy of enforcement discretion does not apply to commercial operations such as Rx Depot/Rx Canada.
See
Pl.Ex. 21.
20. Moreover, the Supreme Court has held that “an agency’s decision not to prosecute or enforce, whether through civil or
criminal process, is a decision to an agency’s absolute discretion.”
Heckler v. Chaney,
470 U.S. 821, 831, 105 S.Ct. 1649, 84 L.Ed.2d 714 (1985). To prevail on a claim of selective prosecution, therefore, the defendants must show that others similarly situated have not been subject to enforcement proceedings by the government, and that there was a constitutionally impermissible basis for the decision to institute enforcement action against the defendants such as race, religion, or other arbitrary classification.
United States v. Armstrong,
517 U.S. 456, 464-65, 116 S.Ct. 1480, 134 L.Ed.2d 687 (1996) (citing
Oyler v. Boles,
368 U.S. 448, 456, 82 S.Ct. 501, 7 L.Ed.2d 446 (1962));
Wayte v. United States,
470 U.S. 598, 608, 105 S.Ct. 1524, 84 L.Ed.2d 547 (1985). Defendants have made no such showing here. Instead, the defendants point to FDA’s failure to prosecute all individuals who cross the Canadian border on their own or use the Internet to buy their prescription drugs. Defendants claim that this fact evidences some vague policy of “geographical” discrimination. It is reasonable, however, for FDA to marshal its limited resources against large-scale, commercial operations such as Rx Depot/Rx Canada rather than small-scale, individual violators.
21. The Congressional intent referred to in Findings of Fact 41 and 45,
supra,
expressly conditioned the implementation of the MEDS Act on a determination by the Secretary of Health and Human Services that the envisioned new system would pose no additional health risks to U.S. consumers, and that it would result in significant cost savings to the American public. 21 U.S.C. § 384(1). The current and previous HHS secretaries have not made such a determination. Pl.Ex. 22; Trans, at 133,139.
E.
Defendants’Remaining Claims
22. Defendants’ remaining arguments and counterclaims similarly do not justify affirmative relief nor do they override plaintiffs interest in enforcing the law.
23. Defendants argue that plaintiffs enforcement actions violate the Privileges and Immunities Clause, U.S. Const., art. IV, § 2. The Privileges and Immunities Clause does not apply here; the Clause requires a State to accord residents and non-residents equal treatment when regulating the means of livelihood or doing business. In any event, the defendants have not shown that they have a privilege or fundamental right to facilitate illegal prescription drug importation.
See Supreme Court of New Hampshire v. Piper,
470 U.S. 274, 279, 105 S.Ct. 1272, 84 L.Ed.2d 205 (1985).
24. Likewise, the facilitation of such imports, even to the extent it involves “speech,” is not protected by the First Amendment.
See United States v. Pinelli,
890 F.2d 1461, 1472 (10th Cir.1989) (illegal conduct not protected'simply because it involves speech) (citing
Giboney v. Empire Storage & Ice Co.,
336 U.S. 490, 502, 69 S.Ct. 684, 93 L.Ed. 834 (1949));
Pittsburgh Press Co. v. Pittsburgh Comm’n on Human Relations,
413 U.S. 376, 389, 93 S.Ct. 2553, 37 L.Ed.2d 669 (1973) (any First Amendment interest in advertising a commercial transaction is “altogether absent when the commercial activity itself is illegal and the restriction on advertising is incidental to a valid limitation on economic activity.”).
25. The North American Free Trade Agreement, as defendants conceded at the hearing, provides no remedy to private citizens. 19 U.S.C. § 3312(c); Trans, at 13.
26. Finally, the Court’s equitable powers are
not
appropriately invoked. It would be an abuse of the Court’s equitable power to ignore statutory law, or to declare a statute invalid where there is no constitutional basis for doing so. “A district court cannot ... override Congress’ policy choice, articulated in a statute, as to what behavior should be prohibited. ‘Once Congress, exercising its delegated powers, has decided the order of priorities in a given area, it is ... for the courts to enforce them when enforcement is sought.’ ”
United States v. Oakland Cannabis Buyers’ Co-op.,
532 U.S. 483, 497, 121 S.Ct. 1711, 149 L.Ed.2d 722 (2001) (quoting
TVA v. Hill,
437 U.S.
153, 194, 98
S.Ct. 2279, 57 L.Ed.2d 117 (1978)).
III.
CONCLUSION
27. FDA warned the defendants that their violations would subject them to enforcement action. Notwithstanding this warning, the defendants failed to comply with the FDCA; in fact, they expanded their operations. Unless restrained by order of this Court, the defendants will continue to violate 21 U.S.C. §§ 331(d) and (t).
28. Plaintiffs motion for a preliminary injunction (Dkt.# 2) is granted.
29. For the same reasons described herein, defendants’ motion for a preliminary injunction (Dkt.# 10) is denied.
30. Plaintiffs motion in limine (Dkt.# 11) is granted as to lay testimony regarding safety and effectiveness of particular drugs, and denied as moot as to all other evidence sought to be excluded.
31. Any finding of fact which is more appropriately characterized as a conclusion of law is incorporated herein.
ORDER OF PRELIMINARY INJUNCTION
Plaintiff, United States of America, having filed a complaint for injunction and a motion for preliminary injunction against defendants Rx Depot, Inc. and Rx of Canada, LLC, corporations, and Carl Moore and David Peoples, individuals (collectively “defendants”); and defendants having-filed their own motion for preliminary injunction; and the Court having heard the evidence at a hearing on October 8-9, 2003; and the Court having considered the pleadings, the evidence, and arguments of counsel, and having entered its findings of fact and conclusions of law simultaneously herewith; and it appearing that the defendants are violating and, unless restrained by order of this Court, will continue to violate the Federal Food, Drug, and Cosmetic Act (the “Act”), 21 U.S.C. §§ 331(t) and (d), by importing, or causing importation of, drugs in violation of 21 U.S.C. § 381(d)(1), and by introducing or delivering for introduction, or causing to be introduced or delivered, into interstate commerce unapproved new drugs; and it appearing that, despite repeated warnings that their actions violate the law, the defendants will not stop these illegal practices unless enjoined by the Court; and it appearing that the defendants’ practices expose the public health to risk.
IT IS HEREBY ORDERED, ADJUDGED, AND DECREED that:
1. This Court has jurisdiction over the subject matter herein and has personal jurisdiction over all parties to this action.
2. The complaint for injunction states a cause of action against the defendants under the Act, 21 U.S.C. § 301
et seq.
3. There is a substantial likelihood that plaintiff will succeed on the merits of its claim that the defendants violate 21 U.S.C. § 331(t), by importing, or causing to be imported, into the United States drugs that were manufactured in the United States by persons other than the defendants, in violation of 21 U.S.C. § 381(d)(1).
4. There is a substantial likelihood that plaintiff will succeed on the merits of its claim that the defendants violate 21 U.S.C. § 331(d), by doing or causing the introduction or delivery for introduction into interstate commerce of drugs that are new drugs within the meaning of 21 U.S.C. § 321(p), that have not been approved by the Food and Drug Administration (“FDA”), in violation of 21 U.S.C. § 355(a).
5. The defendants and each and all of their officers, agents, representatives, employees, successors, assigns, attorneys, and any and all persons in active concert or participation with any of them (including franchisees, affiliates, and “doing business as” entities) who have received actual notice of this Order by personal service or otherwise, are hereby preliminarily restrained and enjoined under 21 U.S.C. § 332(a), from directly or indirectly doing or causing, during the pendency of this action, the introduction, or delivery for introduction, into interstate commerce, including, but not limited to, the importation of, any article of drug, and from directly or indirectly receiving any commission associated with the refill of any prescription.
6. Upon the entry of this Order, the persons and entities identified in the preceding paragraph shall cease offering, advertising, or promoting, through any media, including, but not limited to, the websites www.rxdepot.com and wwwrxof-canada.net, any service that causes or facilitates the importation or assistance in importing articles of drug from any place outside the United States.
7. Within 10 calendar days of entry of this Order, the defendants shall send a letter, which must be approved in advance in writing by FDA, to all of their customers notifying them that the defendants’ business violates the law and that the safety, purity, and efficacy of drug products obtained through the defendants cannot be assured.
8. Representatives of FDA shall be permitted, without prior notice and as and when FDA deems necessary, to make inspections of the defendants’ facilities and, without prior notice, take any other measures necessary to monitor and ensure continuing compliance with the terms of this Order. During such inspections, FDA investigators shall be permitted access to all equipment, finished and unfinished drugs, and all labeling, including promotional materials and website information; to take photographs and make video recordings; to take samples of the defendants’ finished and unfinished materials and products, containers, and labeling; and to examine and copy all records relating to product formulation, adverse reactions, complaints, the relationship between defendants and their franchisees, affiliates, and “doing business as” entities, the ordering of prescription drugs from Canada and any other countries, and the receipt, processing, labeling, packing, manufacture, and distribution of any product. Such inspections shall be permitted upon presentation of a copy of this Order and appropriate credentials. The inspection authority granted by this Order is apart from, and in addition to, the authority to conduct inspections under 21 U.S.C. § 374.
9. The defendants shall provide a copy of this Order, by personal service or registered mail, within 10 calendar days of its entry, to each of their officers, agents, representatives, employees, successors, assigns, attorneys, and any and all persons in active concert or participation with any of them (including all franchisees, affiliates, and “doing business as” entities). The defendants shall provide an affidavit of compliance, signed by a person with personal knowledge of the facts, stating the fact and manner of compliance with the first sentence of this paragraph, and identifying the names and positions of all
persons so notified, to FDA within 30 calendar days after the date of entry of this Order. All physical locations and websites shall be identified as such in this written affidavit to FDA.
10. If the defendants or any of their officers, agents, representatives, employees, successors, assigns, attorneys, and any and all persons in active concert or participation with any of them (including, but not limited to, franchisees, affiliates, and “doing business as” entities) violate this Order and are found in civil or criminal contempt thereof, the defendants shall, in addition to other remedies, pay attorney fees, travel expenses incurred by attorneys and witnesses, court costs, expert witness fees, and investigational and analytical expenses incurred by plaintiff in bringing such action.