Product NDC: | 60760-145 |
Proprietary Name: | CARVEDILOL |
Non Proprietary Name: | CARVEDILOL |
Active Ingredient(s): | 25 mg/1 & nbsp; CARVEDILOL |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60760-145 |
Labeler Name: | St Marys Medical Park Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078332 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130425 |
Package NDC: | 60760-145-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-145-60) |
NDC Code | 60760-145-60 |
Proprietary Name | CARVEDILOL |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-145-60) |
Product NDC | 60760-145 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CARVEDILOL |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130425 |
Marketing Category Name | ANDA |
Labeler Name | St Marys Medical Park Pharmacy |
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] |