US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 6, 2020 (6 years ago)

clomiPRAMINE Hydrochloride Capsules USP, 50 mg, 30-count bottle, Rx Only, Manufactured…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Tablet/Capsule Specification

What was recalled

clomiPRAMINE Hydrochloride Capsules USP, 50 mg, 30-count bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD NDC 59746-711-30

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-711-30
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0104-2021

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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