FDA Drug Recalls

Recalls / Brands / Clomipramine Hydrochloride

Clomipramine Hydrochloride

6 FDA drug recalls involving brand “Clomipramine Hydrochloride.

DateClassProductFirm
2025-10-22Class IIclomiPRAMINE Hydrochloride, Capsules, USP, 25 mg, packaged in a) 30-count bottles (NDC 16714-849-01), b) 90-coZydus Pharmaceuticals (USA) Inc
2025-10-22Class IIclomiPRAMINE Hydrochloride, Capsules, USP, 50 mg, packaged in a) 30-count bottles (NDC 16714-850-01), b) 90-coZydus Pharmaceuticals (USA) Inc
2025-10-22Class IIclomiPRAMINE Hydrochloride, Capsules, USP, 75 mg, packaged in a) 30-count bottles (NDC 16714-851-01), b) 90-coZydus Pharmaceuticals (USA) Inc
2025-06-27Class IIclomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, NapleLupin Pharmaceuticals Inc.
2025-04-10Class IIclomiPRAMINE hydrochloride Capsules USP, 25 mg, 100-count bottle, Rx only, Manufactured For: Lupin PharmaceutiLupin Pharmaceuticals Inc.
2022-08-23Class IIIClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA, Manufactured by: LeLeading Pharma, LLC