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Hydrochlorothiazide - 29300-128-00 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 29300-128
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: 29300-128
Labeler Name: Unichem Pharmaceuticals (USA), Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040907
Marketing Category: ANDA
Start Marketing Date: 20090702

Package Information of Hydrochlorothiazide

Package NDC: 29300-128-00
Package Description: 150000 TABLET in 1 DRUM (29300-128-00)

NDC Information of Hydrochlorothiazide

NDC Code 29300-128-00
Proprietary Name Hydrochlorothiazide
Package Description 150000 TABLET in 1 DRUM (29300-128-00)
Product NDC 29300-128
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090702
Marketing Category Name ANDA
Labeler Name Unichem Pharmaceuticals (USA), 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


General Information