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Irbesartan and Hydrochlorothiazide - 65862-629-90 - (Irbesartan and Hydrochlorothiazide)

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Drug Information of Irbesartan and Hydrochlorothiazide

Product NDC: 65862-629
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: 65862-629
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203630
Marketing Category: ANDA
Start Marketing Date: 20130222

Package Information of Irbesartan and Hydrochlorothiazide

Package NDC: 65862-629-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (65862-629-90)

NDC Information of Irbesartan and Hydrochlorothiazide

NDC Code 65862-629-90
Proprietary Name Irbesartan and Hydrochlorothiazide
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (65862-629-90)
Product NDC 65862-629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130222
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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