NDC Code | 51407-041-01 |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-041-01) |
Product NDC | 51407-041 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Carvedilol |
Non-Proprietary Name | Carvedilol |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20070905 |
Marketing Category Name | ANDA |
Application Number | ANDA078384 |
Manufacturer | Golden State Medical Supply, Inc. |
Substance Name | CARVEDILOL |
Strength | 12.5 |
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] |