Drug recall D-0451-2022
Product
Metoprolol Succinate Extended-Release Tablets, USP 50 mg, 500-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013 INDIA. NDC 68001-501-03
Reason for recall
Failed Dissolution Specifications
Lots and codes
Lots# 21141983, 21141984 and 21141985, Exp 03/31/2023; Lots# 21142017, 21142018, 21142019, Exp 02/28/2023
Recall details
- Recalling firm
- American Health Packaging, Columbus, OH
- Quantity
- 6,637 500-count bottles
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- December 20, 2021
- Terminated
- March 9, 2023
Related products
- Metoprolol Succinate – drug information
- NDC 68001-501 Metoprolol Succinate · Metoprolol Succinate 50 mg/1 · BluePoint Laboratories
- NDC 68001-503 Metoprolol Succinate · Metoprolol Succinate 200 mg/1 · BluePoint Laboratories
- NDC 68001-502 Metoprolol Succinate · Metoprolol Succinate 100 mg/1 · BluePoint Laboratories
- NDC 68001-500 Metoprolol Succinate · Metoprolol Succinate 25 mg/1 · BluePoint Laboratories