NDC Code | 60429-141-01 |
Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-141-01) |
Product NDC | 60429-141 |
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 | 20100415 |
Marketing Category Name | ANDA |
Application Number | ANDA077298 |
Manufacturer | Golden State Medical Supply, Inc. |
Substance Name | METOPROLOL SUCCINATE |
Strength | 100 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |