AVAPRO - 0087-2771-32 - (IRBESARTAN)

Alphabetical Index


Drug Information of AVAPRO

Product NDC: 0087-2771
Proprietary Name: AVAPRO
Non Proprietary Name: IRBESARTAN
Active Ingredient(s): 75    mg/1 & nbsp;   IRBESARTAN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of AVAPRO

Product NDC: 0087-2771
Labeler Name: Bristol-Myers Squibb Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020757
Marketing Category: NDA
Start Marketing Date: 19970930

Package Information of AVAPRO

Package NDC: 0087-2771-32
Package Description: 90 TABLET in 1 BOTTLE (0087-2771-32)

NDC Information of AVAPRO

NDC Code 0087-2771-32
Proprietary Name AVAPRO
Package Description 90 TABLET in 1 BOTTLE (0087-2771-32)
Product NDC 0087-2771
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 Bristol-Myers Squibb Company
Substance Name IRBESARTAN
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of AVAPRO


General Information