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Hydrochlorothiazide - 50436-3922-1 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 50436-3922
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: 50436-3922
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084325
Marketing Category: ANDA
Start Marketing Date: 20070501

Package Information of Hydrochlorothiazide

Package NDC: 50436-3922-1
Package Description: 30 TABLET in 1 BOTTLE (50436-3922-1)

NDC Information of Hydrochlorothiazide

NDC Code 50436-3922-1
Proprietary Name Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE (50436-3922-1)
Product NDC 50436-3922
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070501
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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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