Carvedilol - 49349-112-20 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 49349-112
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)

Labeler Information of Carvedilol

Product NDC: 49349-112
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076649
Marketing Category: ANDA
Start Marketing Date: 20130415

Package Information of Carvedilol

Package NDC: 49349-112-20
Package Description: 100 TABLET, FILM COATED in 1 CANISTER (49349-112-20)

NDC Information of Carvedilol

NDC Code 49349-112-20
Proprietary Name Carvedilol
Package Description 100 TABLET, FILM COATED in 1 CANISTER (49349-112-20)
Product NDC 49349-112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130415
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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]

Complete Information of Carvedilol


General Information