| NDC Code | 53002-4561-1 |
|---|
| Package Description | 10 TABLET in 1 BOTTLE (53002-4561-1) |
|---|
| Product NDC | 53002-4561 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19860513 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA070175 |
|---|
| Manufacturer | RPK Pharmaceuticals, Inc. |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|