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Hydrochlorothiazide - 52959-132-00 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 52959-132
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: 52959-132
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040807
Marketing Category: ANDA
Start Marketing Date: 20100820

Package Information of Hydrochlorothiazide

Package NDC: 52959-132-00
Package Description: 100 TABLET in 1 BOTTLE (52959-132-00)

NDC Information of Hydrochlorothiazide

NDC Code 52959-132-00
Proprietary Name Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE (52959-132-00)
Product NDC 52959-132
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100820
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
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


General Information