| NDC Code | 51655-580-52 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, DISPENSING (51655-580-52) |
|---|
| Product NDC | 51655-580 |
|---|
| 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 | 20140507 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076862 |
|---|
| Manufacturer | Northwind Pharmaceuticals |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/301 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|