Irbesartan - 68180-410-09 - (Irbesartan)

Alphabetical Index


Drug Information of Irbesartan

Product NDC: 68180-410
Proprietary Name: Irbesartan
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 Irbesartan

Product NDC: 68180-410
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201531
Marketing Category: ANDA
Start Marketing Date: 20121023

Package Information of Irbesartan

Package NDC: 68180-410-09
Package Description: 90 TABLET in 1 BOTTLE (68180-410-09)

NDC Information of Irbesartan

NDC Code 68180-410-09
Proprietary Name Irbesartan
Package Description 90 TABLET in 1 BOTTLE (68180-410-09)
Product NDC 68180-410
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121023
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
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 Irbesartan


General Information