| NDC Code | 31722-592-05 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-592-05) |
|---|
| Product NDC | 31722-592 |
|---|
| 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 | 20201106 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205541 |
|---|
| Manufacturer | Camber Pharmaceuticals, Inc. |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|