AVAPRO - 63629-3373-4 - (IRBESARTAN)

Alphabetical Index


Drug Information of AVAPRO

Product NDC: 63629-3373
Proprietary Name: AVAPRO
Non Proprietary Name: IRBESARTAN
Active Ingredient(s): 150    mg/1 & nbsp;   IRBESARTAN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of AVAPRO

Product NDC: 63629-3373
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020757
Marketing Category: NDA
Start Marketing Date: 19970930

Package Information of AVAPRO

Package NDC: 63629-3373-4
Package Description: 180 TABLET in 1 BOTTLE (63629-3373-4)

NDC Information of AVAPRO

NDC Code 63629-3373-4
Proprietary Name AVAPRO
Package Description 180 TABLET in 1 BOTTLE (63629-3373-4)
Product NDC 63629-3373
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IRBESARTAN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970930
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name IRBESARTAN
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of AVAPRO


General Information