Carvedilol - 0615-6585-39 - (Carvedilol)

Alphabetical Index


Drug Information of Carvedilol

Product NDC: 0615-6585
Proprietary Name: Carvedilol
Non Proprietary Name: Carvedilol
Active Ingredient(s): 12.5    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: 0615-6585
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078227
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of Carvedilol

Package NDC: 0615-6585-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6585-39)

NDC Information of Carvedilol

NDC Code 0615-6585-39
Proprietary Name Carvedilol
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6585-39)
Product NDC 0615-6585
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 NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name CARVEDILOL
Strength Number 12.5
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