| NDC Code | 68001-501-08 |
|---|
| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-08) |
|---|
| Product NDC | 68001-501 |
|---|
| 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 | 20210514 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211143 |
|---|
| Manufacturer | BluePoint Laboratories |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|