Galt Pharmaceuticals LLC

CLOSEOUT LETTER Galt Pharmaceuticals LLC MARCS-CMS 593156 — June 03, 2020 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Drugs Recipient: Recipient Name Manoj Amaraneni Recipient Title Regulatory Affairs Officer Galt Pharmaceuticals LLC 3350 Riverwood Parkway Suite 1900 Atlanta , GA 30339 United States Issuing Office: Division of Advertising & Promotion Review United States Dear Mr. Amaraneni: The Food and Drug Administration has completed evaluation of your firm’s corrective actions in response to our Warning Letter dated September 13, 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 51 in addition to the NDA number in all future correspondence relating to this particular matter. Sincerely, {See appended electronic signature page} Christine Bradshaw, Pharm D, RAC Regulatory Review Officer Division of Advertising & Promotion Review 1 Office of Prescription Drug Promotion Reference ID: 4618801 -------------------------------------------------------------------------------------------- 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: 06/12/2020 Regulated Product(s) Drugs