Product NDC: | 55154-1389 |
Proprietary Name: | Carvedilol |
Non Proprietary Name: | Carvedilol |
Active Ingredient(s): | 25 mg/1 & nbsp; Carvedilol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-1389 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078251 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100604 |
Package NDC: | 55154-1389-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-1389-0) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 55154-1389-0 |
Proprietary Name | Carvedilol |
Package Description | 10 BLISTER PACK in 1 BAG (55154-1389-0) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 55154-1389 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Carvedilol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100604 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | CARVEDILOL |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC] |