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Hydrochlorothiazide - 55289-135-01 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 55289-135
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: 55289-135
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040412
Marketing Category: ANDA
Start Marketing Date: 20020329

Package Information of Hydrochlorothiazide

Package NDC: 55289-135-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (55289-135-01)

NDC Information of Hydrochlorothiazide

NDC Code 55289-135-01
Proprietary Name Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (55289-135-01)
Product NDC 55289-135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020329
Marketing Category Name ANDA
Labeler Name PD-Rx 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


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