Irbesartan - 0591-2783-30 - (Irbesartan)

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Drug Information of Irbesartan

Product NDC: 0591-2783
Proprietary Name: Irbesartan
Non Proprietary Name: Irbesartan
Active Ingredient(s): 150    mg/1 & nbsp;   Irbesartan
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Irbesartan

Product NDC: 0591-2783
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090720
Marketing Category: ANDA
Start Marketing Date: 20121016

Package Information of Irbesartan

Package NDC: 0591-2783-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (0591-2783-30)

NDC Information of Irbesartan

NDC Code 0591-2783-30
Proprietary Name Irbesartan
Package Description 30 TABLET, COATED in 1 BOTTLE (0591-2783-30)
Product NDC 0591-2783
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121016
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
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