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HYDROCHLOROTHIAZIDE - 16590-294-60 - (HYDROCHLOROTHIAZIDE)

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Drug Information of HYDROCHLOROTHIAZIDE

Product NDC: 16590-294
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: 16590-294
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083177
Marketing Category: ANDA
Start Marketing Date: 20100402

Package Information of HYDROCHLOROTHIAZIDE

Package NDC: 16590-294-60
Package Description: 60 TABLET in 1 BOTTLE (16590-294-60)

NDC Information of HYDROCHLOROTHIAZIDE

NDC Code 16590-294-60
Proprietary Name HYDROCHLOROTHIAZIDE
Package Description 60 TABLET in 1 BOTTLE (16590-294-60)
Product NDC 16590-294
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100402
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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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