Amneal Pharmaceuticals recalls 200mg chlorproMAZINE tablets due to micro-organism in packaging material. No tablets were contaminated. Affected lots: AM240336, AM240337 (expiring 02/2027).
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.
Amneal Pharmaceuticals is recalling 200mg chlorproMAZINE Hydrochloride tablets that may contain a foreign micro-organism in their packaging. This could pose a risk if the packaging is compromised, but the tablets themselves are not contaminated. The recall affects specific lots manufactured in India with an expiration date of February 2027.
A specific type of packaging material used in the tablets' containers was found to contain a micro-organism. However, the actual tablets themselves do not have any micro-organism contamination. This means the risk is limited to the packaging material being compromised.
Prescription owners of the 200mg chlorproMAZINE tablets with lot numbers AM240336 or AM240337. People taking these medications for conditions like anxiety or insomnia are most at risk if the packaging is damaged.
Check for lot numbers AM240336 or AM240337 on the packaging. The tablets are prescription-only 200mg chlorproMAZINE Hydrochloride, 100-count bottles manufactured in India with an expiration date of February 2027.
Look for lot numbers AM240336 or AM240337 on the tablet packaging.
No, the tablets themselves do not contain microorganisms. The issue is with the packaging material.
The recall record does not specify a remedy, so no action is required beyond checking the lot numbers.
The recalled tablets expire on February 28, 2027.
We’ve drafted a message you can send Amneal Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0619-2025 — Amneal Pharmaceuticals Amneal Pharmaceuticals Hello, I own a Amneal Pharmaceuticals that is covered by recall D-0619-2025 from Amneal Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
