Irbesartan - 31722-731-31 - (Irbesartan)

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Drug Information of Irbesartan

Product NDC: 31722-731
Proprietary Name: Irbesartan
Non Proprietary Name: Irbesartan
Active Ingredient(s): 300    mg/1 & nbsp;   Irbesartan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Irbesartan

Product NDC: 31722-731
Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202910
Marketing Category: ANDA
Start Marketing Date: 20120927

Package Information of Irbesartan

Package NDC: 31722-731-31
Package Description: 120 BLISTER PACK in 1 CARTON (31722-731-31) > 10 TABLET in 1 BLISTER PACK

NDC Information of Irbesartan

NDC Code 31722-731-31
Proprietary Name Irbesartan
Package Description 120 BLISTER PACK in 1 CARTON (31722-731-31) > 10 TABLET in 1 BLISTER PACK
Product NDC 31722-731
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 Camber Pharmaceuticals, Inc.
Substance Name IRBESARTAN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Irbesartan


General Information