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Hydrochlorothiazide - 67253-821-55 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 67253-821
Proprietary Name: Hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 50    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrochlorothiazide

Product NDC: 67253-821
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087068
Marketing Category: ANDA
Start Marketing Date: 19801105

Package Information of Hydrochlorothiazide

Package NDC: 67253-821-55
Package Description: 5000 TABLET in 1 BOTTLE (67253-821-55)

NDC Information of Hydrochlorothiazide

NDC Code 67253-821-55
Proprietary Name Hydrochlorothiazide
Package Description 5000 TABLET in 1 BOTTLE (67253-821-55)
Product NDC 67253-821
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19801105
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Hydrochlorothiazide


General Information