Carvedilol - 60505-2607-0 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 60505-2607
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: 60505-2607
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078165
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of Carvedilol

Package NDC: 60505-2607-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2607-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Carvedilol

NDC Code 60505-2607-0
Proprietary Name Carvedilol
Package Description 10 BLISTER PACK in 1 CARTON (60505-2607-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-2607
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070905
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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


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