US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 23, 2022 (4 years ago)

ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules

What was recalled

ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-167-01

Recalling firm
Leading Pharma, LLC
NDC code
69315-167-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1546-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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