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Hydrochlorothiazide - 59762-1736-2 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 59762-1736
Proprietary Name: Hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 25    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrochlorothiazide

Product NDC: 59762-1736
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040780
Marketing Category: ANDA
Start Marketing Date: 20070720

Package Information of Hydrochlorothiazide

Package NDC: 59762-1736-2
Package Description: 100 TABLET in 1 BOTTLE (59762-1736-2)

NDC Information of Hydrochlorothiazide

NDC Code 59762-1736-2
Proprietary Name Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE (59762-1736-2)
Product NDC 59762-1736
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070720
Marketing Category Name ANDA
Labeler Name Greenstone LLC
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Hydrochlorothiazide


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