Drug recall D-0216-2025
Product
Carvedilol Tablets, USP, 12.5 mg, Rx only, a)500 Tablets, NDC 68462-164-05; b) 100 Tablets, NDC 68462-164-01, Manufactured for Glenmark Pharmaceuticals, NJ.
Reason for recall
CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit.
Lots and codes
Lot numbers: a) 17230658, Exp.: 02/2025; 17230814,17230822, Exp.: 03/2025; 17231004,17231009,17231022, Exp.: 04/2025; 17231393,17231392, Exp.: 05/2025; 17231538, 17231541,17231542, Exp.: 06/2025; 17231710,17231718,17231721,17231722,17231730, Exp': 07/2025; 17232169, Exp.: 09/2025; 17232253, Exp.: 10/2025; 17240220,17240240, Exp.: 01/2026; 17240459, Exp.: 02/2026 b) 17230814, Exp.: 03/2025; 17231392, Exp.:05/2025; 17232260, Exp.: 10/2025.
Recall details
- Recalling firm
- Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ
- Distribution
- Nationwide in the U.S
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 22, 2025
Related products
- Carvedilol – drug information
- NDC 68462-164 Carvedilol · Carvedilol 12.5 mg/1 · Glenmark Pharmaceuticals Inc., USA
- NDC 68462-163 Carvedilol · Carvedilol 6.25 mg/1 · Glenmark Pharmaceuticals Inc., USA
- NDC 68462-165 Carvedilol · Carvedilol 25 mg/1 · Glenmark Pharmaceuticals Inc., USA
- NDC 68462-162 Carvedilol · Carvedilol 3.125 mg/1 · Glenmark Pharmaceuticals Inc., USA