| NDC Code | 0904-6169-05 |
|---|
| Package Description | 10 BOX, UNIT-DOSE in 1 CARTON (0904-6169-05) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-6169-61) |
|---|
| Product NDC | 0904-6169 |
|---|
| 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 | 20101005 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090615 |
|---|
| Manufacturer | Major Pharmaceuticals |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|