Recall
FDAHealthNovember 1, 2024

Glenmark Pharmaceuticals Inc., USA — Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Rx Only, 100 Capsules, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Produ

⚠️ cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
November 1, 2024

Nationwide in the USA

What's affected?

Product
Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Rx Only, 100 Capsules, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-562-01.
UPC
0368462562017
Lot code
17222470

Additional details

Lot #: 17222470, 17230680, 17222547, Exp. Date 11/30/2024; 17230304, Exp. Date, 12/31/2024; 17230598, Exp. Date, 02/2025.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 25584 bottles.

View original FDA notice →

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