Carvedilol - 0093-0135-05 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 0093-0135
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: 0093-0135
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076373
Marketing Category: ANDA
Start Marketing Date: 20070906

Package Information of Carvedilol

Package NDC: 0093-0135-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-0135-05)

NDC Information of Carvedilol

NDC Code 0093-0135-05
Proprietary Name Carvedilol
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0093-0135-05)
Product NDC 0093-0135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070906
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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