U.S. flag An official website of the United States government

On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.

U.S. Food and Drug Administration
  1. Home
  2. Inspections, Compliance, Enforcement, and Criminal Investigations
  3. Compliance Actions and Activities
  4. Warning Letters
  5. Metuchen Pharmaceuticals, LLC - 590713 - 09/18/2020
  1. Warning Letters

CLOSEOUT LETTER

Metuchen Pharmaceuticals, LLC MARCS-CMS 590713 —

Reference #:
NDA 202276
Product:
Drugs
Recipient:
Recipient Name
Fady Boctor
Metuchen Pharmaceuticals, LLC

200 US Hwy 9 Suite 500
Manalapan, NJ 07726
United States

Issuing Office:
Office of Prescription Drug Promotion

United States

Dear Mr. Boctor:

The Food and Drug Administration has completed evaluation of your firm’s corrective actions in response to our Warning Letter dated August 16, 2019. Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA surveillance will further assess the adequacy and sustainability of these corrections.

This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during subsequent surveillance or through other means.

If you have any questions or comments, please direct your response to the undersigned at the Food and Drug Administration, Center for Drug Evaluation and Research, Office of Prescription Drug Promotion, 5901-B Ammendale Road, Beltsville, Maryland 20705- 1266. A courtesy copy can be sent by facsimile to (301) 847-8444. To ensure timely delivery of your submissions, please use the full address above and include a prominent directional notation (e.g. a sticker) to indicate that the submission is intended for OPDP.

Please refer to MA 169, 182, 187 in addition to the NDA number in all future correspondence relating to this particular matter.

Sincerely,
{See appended electronic signature page}
Elvy Varghese, PharmD
Regulatory Review Officer
Division of Advertising & Promotion Review 2
Office of Prescription Drug Promotion

Cc: Nicol George, PharmD
      Executive Director, Regulatory & Medical Review Services
      OneSource Regulatory LLC
      PO Box 1047
      Libertyville, IL 60048

--------------------------------------------------------------------------------------------
This is a representation of an electronic record that was signed
electronically. Following this are manifestations of any and all
electronic signatures for this electronic record.
--------------------------------------------------------------------------------------------
/s/
------------------------------------------------------------
ELVY M VARGHESE
09/18/2020 10:03:33 AM

Back to Top