Class II
Ongoing
Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ, 07430, Product of India, NDC 68462-562-01.
This recall is currently active, issued May 1, 2024. It was issued by Glenmark Pharmaceuticals Inc., Usa.
- Recall Initiated
- April 17, 2024
- Posted
- May 1, 2024
- Recall Number
- D-0472-2024
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 3,264 bottles
- Firm Location
- Mahwah, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Dissolution Specifications
Distribution
Nationwide in the USA.
Lot / Code Info
Lot #: 17221312, Exp. 5/31/2024
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