Irbesartan - 0093-7464-56 - (Irbesartan)

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Drug Information of Irbesartan

Product NDC: 0093-7464
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: 0093-7464
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077159
Marketing Category: ANDA
Start Marketing Date: 20120330

Package Information of Irbesartan

Package NDC: 0093-7464-56
Package Description: 30 TABLET in 1 BOTTLE (0093-7464-56)

NDC Information of Irbesartan

NDC Code 0093-7464-56
Proprietary Name Irbesartan
Package Description 30 TABLET in 1 BOTTLE (0093-7464-56)
Product NDC 0093-7464
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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