Carvedilol - 55154-1389-0 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 55154-1389
Proprietary Name: Carvedilol
Non Proprietary Name: Carvedilol
Active Ingredient(s): 25    mg/1 & nbsp;   Carvedilol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carvedilol

Product NDC: 55154-1389
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078251
Marketing Category: ANDA
Start Marketing Date: 20100604

Package Information of Carvedilol

Package NDC: 55154-1389-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1389-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Carvedilol

NDC Code 55154-1389-0
Proprietary Name Carvedilol
Package Description 10 BLISTER PACK in 1 BAG (55154-1389-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-1389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100604
Marketing Category Name ANDA
Labeler Name Cardinal Health
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