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Hydrochlorothiazide - 16590-293-90 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 16590-293
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: 16590-293
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040412
Marketing Category: ANDA
Start Marketing Date: 20020329

Package Information of Hydrochlorothiazide

Package NDC: 16590-293-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (16590-293-90)

NDC Information of Hydrochlorothiazide

NDC Code 16590-293-90
Proprietary Name Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (16590-293-90)
Product NDC 16590-293
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 STAT Rx USA LLC
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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