NDC Code | 68788-8604-6 |
Package Description | 60 TABLET in 1 BOTTLE (68788-8604-6) |
Product NDC | 68788-8604 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Propranolol Hydrochloride |
Non-Proprietary Name | Propranolol Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20240312 |
Marketing Category Name | ANDA |
Application Number | ANDA071972 |
Manufacturer | Preferred Pharmaceuticals Inc. |
Substance Name | PROPRANOLOL HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |