FDA Drug Recalls

Recalls / Generics / Metoprolol Succinate Er Tablets

Metoprolol Succinate Er Tablets

6 FDA drug recalls involving generic “Metoprolol Succinate Er Tablets.

DateClassProductFirm
2023-01-11Class IIMetoprolol Succinate Extended-Release Tablets, USP, 50 mg, packaged in (a) 100-count bottle, NDC 68001-501-00;Amerisource Health Services LLC
2023-01-05Class IIMetoprolol Succinate Extended-Release Tablets, USP 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: AAscend Laboratories, LLC
2023-01-05Class IIMetoprolol Succinate Extended-Release Tablets, USP 50 mg, Rx Only, 100 Tablets per bottle, Manufactured by: AlAscend Laboratories, LLC
2023-01-05Class IIMetoprolol Succinate Extended-Release Tablets, USP 50 mg, Rx Only, 500 Tablets per bottle, Manufactured by: AAscend Laboratories, LLC
2022-01-12Class IIMetoprolol Succinate Extended-Release Tablets, USP, 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: AAscend Laboratories, LLC
2021-12-20Class IIMetoprolol Succinate Extended-Release Tablets, USP 50 mg, 500-count bottle, Rx Only, Manufactured by: Alkem LaAmerican Health Packaging