Carvedilol - 49349-996-24 - (Carvedilol)

Alphabetical Index


Drug Information of Carvedilol

Product NDC: 49349-996
Proprietary Name: Carvedilol
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)

Labeler Information of Carvedilol

Product NDC: 49349-996
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078332
Marketing Category: ANDA
Start Marketing Date: 20130329

Package Information of Carvedilol

Package NDC: 49349-996-24
Package Description: 200 TABLET, FILM COATED in 1 CANISTER (49349-996-24)

NDC Information of Carvedilol

NDC Code 49349-996-24
Proprietary Name Carvedilol
Package Description 200 TABLET, FILM COATED in 1 CANISTER (49349-996-24)
Product NDC 49349-996
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130329
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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]

Complete Information of Carvedilol


General Information