NDC Code | 54868-5564-0 |
Package Description | 60 TABLET in 1 BOTTLE (54868-5564-0) |
Product NDC | 54868-5564 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Propranolol Hydrochloride |
Non-Proprietary Name | Propranolol Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20060330 |
Marketing Category Name | ANDA |
Application Number | ANDA078955 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | PROPRANOLOL HYDROCHLORIDE |
Strength | 60 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |