Irbesartan - 33342-049-39 - (Irbesartan)

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Drug Information of Irbesartan

Product NDC: 33342-049
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: 33342-049
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202254
Marketing Category: ANDA
Start Marketing Date: 20120927

Package Information of Irbesartan

Package NDC: 33342-049-39
Package Description: 9 BLISTER PACK in 1 CARTON (33342-049-39) > 10 TABLET in 1 BLISTER PACK

NDC Information of Irbesartan

NDC Code 33342-049-39
Proprietary Name Irbesartan
Package Description 9 BLISTER PACK in 1 CARTON (33342-049-39) > 10 TABLET in 1 BLISTER PACK
Product NDC 33342-049
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 Macleods Pharmaceuticals Limited
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