Irbesartan - 65862-638-30 - (Irbesartan)

Alphabetical Index


Drug Information of Irbesartan

Product NDC: 65862-638
Proprietary Name: Irbesartan
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 Irbesartan

Product NDC: 65862-638
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203081
Marketing Category: ANDA
Start Marketing Date: 20120927

Package Information of Irbesartan

Package NDC: 65862-638-30
Package Description: 30 TABLET in 1 BOTTLE (65862-638-30)

NDC Information of Irbesartan

NDC Code 65862-638-30
Proprietary Name Irbesartan
Package Description 30 TABLET in 1 BOTTLE (65862-638-30)
Product NDC 65862-638
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120927
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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