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Hydrochlorothiazide - 0172-2089-60 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 0172-2089
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: 0172-2089
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083177
Marketing Category: ANDA
Start Marketing Date: 19800107

Package Information of Hydrochlorothiazide

Package NDC: 0172-2089-60
Package Description: 100 TABLET in 1 BOTTLE (0172-2089-60)

NDC Information of Hydrochlorothiazide

NDC Code 0172-2089-60
Proprietary Name Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE (0172-2089-60)
Product NDC 0172-2089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19800107
Marketing Category Name ANDA
Labeler Name IVAX 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