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Hydrochlorothiazide - 64125-131-50 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 64125-131
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: 64125-131
Labeler Name: Excellium Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040702
Marketing Category: ANDA
Start Marketing Date: 20070601

Package Information of Hydrochlorothiazide

Package NDC: 64125-131-50
Package Description: 5000 TABLET in 1 BOTTLE (64125-131-50)

NDC Information of Hydrochlorothiazide

NDC Code 64125-131-50
Proprietary Name Hydrochlorothiazide
Package Description 5000 TABLET in 1 BOTTLE (64125-131-50)
Product NDC 64125-131
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070601
Marketing Category Name ANDA
Labeler Name Excellium Pharmaceutical 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


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