Carvedilol - 52125-119-02 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 52125-119
Proprietary Name: Carvedilol
Non Proprietary Name: Carvedilol
Active Ingredient(s): 6.25    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: 52125-119
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076373
Marketing Category: ANDA
Start Marketing Date: 20130402

Package Information of Carvedilol

Package NDC: 52125-119-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-119-02)

NDC Information of Carvedilol

NDC Code 52125-119-02
Proprietary Name Carvedilol
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-119-02)
Product NDC 52125-119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130402
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CARVEDILOL
Strength Number 6.25
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