NDC Code | 70010-781-05 |
Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-05) |
Product NDC | 70010-781 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Metoprolol Succinate |
Non-Proprietary Name | Metoprolol Succinate |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20231002 |
Marketing Category Name | ANDA |
Application Number | ANDA216916 |
Manufacturer | Granules Pharmaceuticals Inc. |
Substance Name | METOPROLOL SUCCINATE |
Strength | 50 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |