FDA Letter API

Mikart LLC

Letter data

Company
Mikart LLC
Recipient
Stefano Antonsson | CEO | Mikart LLC | Outlook Pharmaceuticals, Inc. | 8044 Montgomery Road | Suite 700 | Cincinnatti | , | OH | 45236 | United States
Issue date
2021-11-17
Posted date
Not available
FDA office
The Office of Prescription Drug Promotion (OPDP)
Subject
Not available
Product
Drugs
CMS ID
605071
Reference number
ANDA 040776
FEI
Not available
Inspection dates
Not available

Normalized citations

21 CFR: None found

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER Mikart LLC MARCS-CMS 605071 — November 17, 2021 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: TRANSMITTED BY FACSIMILE Reference #: ANDA 040776 Product: Drugs Recipient: Recipient Name Stefano Antonsson Recipient Title CEO Mikart LLC Outlook Pharmaceuticals, Inc. 8044 Montgomery Road Suite 700 Cincinnatti , OH 45236 United States Issuing Office: The Office of Prescription Drug Promotion (OPDP) United States Dear Mr. Antonsson: The Food and Drug Administration has completed evaluation of your firm’s corrective actions in response to our Warning Letter dated February 21, 2020. 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 60 in addition to the ANDA number in all future correspondence relating to this particular matter. Sincerely, {See appended electronic signature page} Domenic D’Alessandro, PharmD, MBA, BCPS Regulatory Review Officer Division of Advertising & Promotion Review 1 Office of Prescription Drug Promotion -------------------------------------------------------------------------------------------- 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/ ------------------------------------------------------------ Content current as of: 12/13/2021 Regulated Product(s) Drugs