Carvedilol - 42291-221-50 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 42291-221
Proprietary Name: Carvedilol
Non Proprietary Name: Carvedilol
Active Ingredient(s): 3.125    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: 42291-221
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078332
Marketing Category: ANDA
Start Marketing Date: 20120319

Package Information of Carvedilol

Package NDC: 42291-221-50
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (42291-221-50)

NDC Information of Carvedilol

NDC Code 42291-221-50
Proprietary Name Carvedilol
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (42291-221-50)
Product NDC 42291-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120319
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name CARVEDILOL
Strength Number 3.125
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