| NDC Code | 54868-0052-0 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (54868-0052-0) |
|---|
| Product NDC | 54868-0052 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20030227 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078955 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|