NDC Code | 68151-0821-8 |
Package Description | 1 mL in 1 BOTTLE (68151-0821-8) |
Product NDC | 68151-0821 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Propranolol Hydrochloride |
Non-Proprietary Name | Propranolol Hydrochloride |
Dosage Form | SOLUTION |
Usage | ORAL |
Start Marketing Date | 19870515 |
Marketing Category Name | ANDA |
Application Number | ANDA070979 |
Manufacturer | Carilion Materials Management |
Substance Name | PROPRANOLOL HYDROCHLORIDE |
Strength | 20 |
Strength Unit | mg/5mL |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |