| NDC Code | 43353-583-60 |
|---|
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43353-583-60) |
|---|
| Product NDC | 43353-583 |
|---|
| 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 | 20090804 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076862 |
|---|
| Manufacturer | Aphena Pharma Solutions - Tennessee, LLC |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|