NDC Code | 0615-7946-30 |
Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7946-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 0615-7946 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Carvedilol |
Non-Proprietary Name | Carvedilol |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20070905 |
End Marketing Date | 20220731 |
Marketing Category Name | ANDA |
Application Number | ANDA078332 |
Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | CARVEDILOL |
Strength | 25 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC] |