Carvedilol - 68788-0999-3 - (Carvedilol)

Alphabetical Index


Drug Information of Carvedilol

Product NDC: 68788-0999
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: 68788-0999
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076649
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of Carvedilol

Package NDC: 68788-0999-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-0999-3)

NDC Information of Carvedilol

NDC Code 68788-0999-3
Proprietary Name Carvedilol
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68788-0999-3)
Product NDC 68788-0999
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 Preferred Pharmaceuticals, 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