| NDC Code | 60429-139-10 |
|---|
| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-139-10) |
|---|
| Product NDC | 60429-139 |
|---|
| 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 | 20090803 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076862 |
|---|
| Manufacturer | Golden State Medical Supply, Inc. |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|