Product NDC: | 67296-0681 |
Proprietary Name: | Carvedilol |
Non Proprietary Name: | Carvedilol |
Active Ingredient(s): | 12.5 mg/1 & nbsp; Carvedilol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67296-0681 |
Labeler Name: | RedPharm Drug Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078251 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070905 |
Package NDC: | 67296-0681-1 |
Package Description: | 60 TABLET in 1 BOTTLE (67296-0681-1) |
NDC Code | 67296-0681-1 |
Proprietary Name | Carvedilol |
Package Description | 60 TABLET in 1 BOTTLE (67296-0681-1) |
Product NDC | 67296-0681 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Carvedilol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070905 |
Marketing Category Name | ANDA |
Labeler Name | RedPharm Drug Inc. |
Substance Name | CARVEDILOL |
Strength Number | 12.5 |
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] |