Inspections, Compliance, Enforcement, and Criminal Investigations
Department of Health and Human Services
|Public Health Service
Food and Drug Administration
|Silver Spring, MD 20993|
October 13, 2009
612 Corporate Way, Suite No.10
Valley Conage, New York 10989
Product: Codeine Sulfate Tablets, 30 mg & 60 mg
Dear Mr. Shah:
This letter is written in reference 10 your firm's marketing or unapproved new drugs in violation or the Federal Food, Drug, and Cosmetic Act (the Act). Based on the information your firm submitted to FDA's Drug Registration and Listing System, you manufacture and distribute the following prescription drugs:
• Codeine Sulfate Tablets, 30 mg
• Codeine Sulfate Tablets, 60 mg
As labeled, the above products are drugs within the meaning of section 201(g)(1)(B) and (C) of the Act [21 U.S.C. §§ 321(g)(1)(B) and (C)] because they are intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease and because they are intended to affect the structure or function of the body. Further, these drug products, as manufactured and distributed by your firm, are "new drugs" within the meaning of section 201(p) or the Act [21 U.S.C. § 321 (p)] because they are not generally recognized as safe and effective for the conditions prescribed, recommended, or suggested in their labeling. Under sections 301 (d) and 505(a) of the Act [21 U.S.C. §§ 331 (d) and 355(a)], a new drug may not be introduced or delivered for introduction into interstate commerce unless an application approved by FDA under either section 505(b) or (j) of the Act [21 U.S.C. § 355(b) or 0)] is in effect for the drug. Based upon our information, there are no FDA-approved applications on file for the above drug products. The marketing of these products without an approved new drug application constitutes a violation of sections 301(d) and 505(a) of the Act.
Additionally, because the above prescription drug products arc intended for conditions that are not amenable to self-diagnosis and treatment by individuals who are not medical practitioners, adequate directions cannot be written for them so that a layman can use the product safely for its Page 2 intended uses, as described in 21 C.F.R. § 201.5. Consequently, their labeling fails to bear adequate directions for their intended uses, causing them to be misbranded under section 502(f)(1) of the Act [21 U.S.C. § 352(f)(1)]. Because your products lack the required approved application, they are not exempt under 21 C.F.R. § 201.115 from the requirements of section 502(f)(1) of the Act. The introduction or delivery for introduction into interstate commerce of these products without approved new drug applications therefore violates sections 301(a) and (d) of the Act [21 U.S.C. §§ 331(a) and (d)].
As described in the guidance entitled "Marketed Unapproved Drugs - Compliance Policy Guide"] the Agency may exercise its enforcement discretion and identify a period of time during which the Agency does not intend to initiate an enforcement action against a currently marketed unapproved drug. FDA does not intend to initiate enforcement actions related to your unapproved drug products, Codeine Sulfate Tablets, 30 mg & 60 mg, which are being manufactured as of the date of this letter, unless the manufacturing of these products continues more than 90 days after the date of this letter. Furthermore, FDA does not intend to initiate enforcement actions related to the shipment in interstate commerce of these products unless they are still being shipped more than 180 days after the date of this letter.
You should be aware that FDA's enforcement discretion will not apply to the following circumstances: (1) if FDA determines that your firm is violating other provisions of the Act; (2) if it appears that your firm, in response to this letter, increases its manufacture or distribution of your unapproved products, Codeine Sulfate Tablets, 30 mg & 60 mg, above your usual volume during these periods; or (3) if FDA learns of new information regarding any serious health risk or hazard associated with codeine sulfate drug products.
The violations cited in this letter are not intended to be an all-inclusive statement of violations that exist in connection with your products. You are responsible for investigating and determining the causes of the violations identified above and for preventing their recurrence or the occurrence of other violations. It is your responsibility to assure that your firm complies with all requirements of Federal law and FDA regulations.
You should take prompt action to correct the violations cited in this letter. Failure to promptly correct these violations may result in legal action without further notice, including, without limitation, seizure and injunction. Other Federal agencies may take this Warning Letter into account when considering the award of contracts.
Within fifteen (15) working days of receipt of this letter, please notify this office in writing regarding whether you plan to cease the violative activities described in this letter. If you no longer manufacture or market the products referenced in this letter, your response should so indicate, including the reasons that, and the date on which, you ceased production. Additionally, if another firm manufactures the products identified above, your reply should include the name and address of the manufacturer. If the firm from which you receive these products is not the manufacturer, please include the name of your supplier in addition to the manufacturer.
Your response to this letter should be directed to the attention of Ms. Astrid Lopez-Goldberg, Regulatory Counsel, at the U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Office of Compliance, W051 RM 5368, 10903 New Hampshire Avenue, Silver Spring, MD 20993.
Michael M. Levy, Jr., Esq.
Division of New Drugs and Labeling Compliance
Office of Compliance
Food and Drug Administration
1 Marketed Unapproved Drugs-Compliance Policy Guide. Available at http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatorylnformation/Guidances/UCM070290.pdf