US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Aug 18, 2025 (13 months ago)

chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottles, Rx Only…

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

Why it was recalled

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

What was recalled

chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottles, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1056-1.

Recalling firm
Amneal Pharmaceuticals, LLC
NDC code
69238-1056-1
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0616-2025

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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