Irbesartan - 0603-4080-32 - (Irbesartan)

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Drug Information of Irbesartan

Product NDC: 0603-4080
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: 0603-4080
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091236
Marketing Category: ANDA
Start Marketing Date: 20120930

Package Information of Irbesartan

Package NDC: 0603-4080-32
Package Description: 1000 TABLET in 1 BOTTLE (0603-4080-32)

NDC Information of Irbesartan

NDC Code 0603-4080-32
Proprietary Name Irbesartan
Package Description 1000 TABLET in 1 BOTTLE (0603-4080-32)
Product NDC 0603-4080
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120930
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
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