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Irbesartan and Hydrochlorothiazide - 0093-8239-56 - (Irbesartan and Hydrochlorothiazide)

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Drug Information of Irbesartan and Hydrochlorothiazide

Product NDC: 0093-8239
Proprietary Name: Irbesartan and Hydrochlorothiazide
Non Proprietary Name: Irbesartan and Hydrochlorothiazide
Active Ingredient(s): 12.5; 300    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: 0093-8239
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077369
Marketing Category: ANDA
Start Marketing Date: 20121214

Package Information of Irbesartan and Hydrochlorothiazide

Package NDC: 0093-8239-56
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-8239-56)

NDC Information of Irbesartan and Hydrochlorothiazide

NDC Code 0093-8239-56
Proprietary Name Irbesartan and Hydrochlorothiazide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0093-8239-56)
Product NDC 0093-8239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Irbesartan and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121214
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name HYDROCHLOROTHIAZIDE; IRBESARTAN
Strength Number 12.5; 300
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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