| NDC Code | 0603-5483-02 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (0603-5483-02) |
|---|
| Product NDC | 0603-5483 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100621 |
|---|
| End Marketing Date | 20180930 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA070218 |
|---|
| Manufacturer | Qualitest Pharmaceuticals |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|