NDC Code | 55700-976-90 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55700-976-90) |
Product NDC | 55700-976 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Metoprolol Succinate |
Non-Proprietary Name | Metoprolol Succinate Er Tablets |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20220719 |
End Marketing Date | 20250930 |
Marketing Category Name | ANDA |
Application Number | ANDA211143 |
Manufacturer | Quality Care Products, LLC |
Substance Name | METOPROLOL SUCCINATE |
Strength | 25 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |