Product NDC: | 49999-938 |
Proprietary Name: | COREG |
Non Proprietary Name: | carvedilol |
Active Ingredient(s): | 12.5 mg/1 & nbsp; carvedilol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-938 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020297 |
Marketing Category: | NDA |
Start Marketing Date: | 20111121 |
Package NDC: | 49999-938-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (49999-938-30) |
NDC Code | 49999-938-30 |
Proprietary Name | COREG |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (49999-938-30) |
Product NDC | 49999-938 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | carvedilol |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20111121 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
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] |