NDC Code | 70518-1654-0 |
Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-1654-0) |
Product NDC | 70518-1654 |
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 | 20181108 |
Marketing Category Name | ANDA |
Application Number | ANDA078703 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | PROPRANOLOL HYDROCHLORIDE |
Strength | 60 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |