Avapro - 0024-5851-30 - (irbesartan)

Alphabetical Index


Drug Information of Avapro

Product NDC: 0024-5851
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: 0024-5851
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020757
Marketing Category: NDA
Start Marketing Date: 20130101

Package Information of Avapro

Package NDC: 0024-5851-30
Package Description: 30 TABLET in 1 BOTTLE (0024-5851-30)

NDC Information of Avapro

NDC Code 0024-5851-30
Proprietary Name Avapro
Package Description 30 TABLET in 1 BOTTLE (0024-5851-30)
Product NDC 0024-5851
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name irbesartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130101
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
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