IRBESARTAN - 60505-3548-8 - (IRBESARTAN)

Alphabetical Index


Drug Information of IRBESARTAN

Product NDC: 60505-3548
Proprietary Name: IRBESARTAN
Non Proprietary Name: IRBESARTAN
Active Ingredient(s): 150    mg/1 & nbsp;   IRBESARTAN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of IRBESARTAN

Product NDC: 60505-3548
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200832
Marketing Category: ANDA
Start Marketing Date: 20121016

Package Information of IRBESARTAN

Package NDC: 60505-3548-8
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (60505-3548-8)

NDC Information of IRBESARTAN

NDC Code 60505-3548-8
Proprietary Name IRBESARTAN
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (60505-3548-8)
Product NDC 60505-3548
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IRBESARTAN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121016
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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 IRBESARTAN


General Information