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Irbesartan and Hydrochlorothiazide - 60505-3603-9 - (Irbesartan and Hydrochlorothiazide)

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Drug Information of Irbesartan and Hydrochlorothiazide

Product NDC: 60505-3603
Proprietary Name: Irbesartan and Hydrochlorothiazide
Non Proprietary Name: Irbesartan and Hydrochlorothiazide
Active Ingredient(s): 12.5; 150    mg/1; mg/1 & nbsp;   Irbesartan and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Irbesartan and Hydrochlorothiazide

Product NDC: 60505-3603
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201505
Marketing Category: ANDA
Start Marketing Date: 20120926

Package Information of Irbesartan and Hydrochlorothiazide

Package NDC: 60505-3603-9
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (60505-3603-9)

NDC Information of Irbesartan and Hydrochlorothiazide

NDC Code 60505-3603-9
Proprietary Name Irbesartan and Hydrochlorothiazide
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (60505-3603-9)
Product NDC 60505-3603
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120926
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name HYDROCHLOROTHIAZIDE; IRBESARTAN
Strength Number 12.5; 150
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Irbesartan and Hydrochlorothiazide


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