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Glenmark Pharmaceuticals Inc., USA: Diltiazem Hydrochloride Extended-Release

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.. Recalled by Glenmark Pharmaceuticals Inc., USA. Distribution: Nationwide in the USA. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot #:17222547, Exp. Date, 11/30/2024; 17230598, Exp. Date 02/28/2025. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who purchased the recalled drug or medication. Return it to the pharmacy where you bought it for a full refund. You generally do not need the original receipt — the pharmacist can look up your purchase history.
Source Official Source ↗
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