NDC Code | 60760-589-30 |
Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-589-30) |
Product NDC | 60760-589 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Propranolol Hydrochloride |
Non-Proprietary Name | Propranolol Hydrochloride |
Dosage Form | CAPSULE, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20130311 |
Marketing Category Name | ANDA |
Application Number | ANDA078703 |
Manufacturer | ST. MARY'S MEDICAL PARK PHARMACY |
Substance Name | PROPRANOLOL HYDROCHLORIDE |
Strength | 80 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |