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Hydrochlorothiazide - 59746-127-10 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 59746-127
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: 59746-127
Labeler Name: JUBILANT CADISTA PHARMACEUTICALS, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040809
Marketing Category: ANDA
Start Marketing Date: 20071026

Package Information of Hydrochlorothiazide

Package NDC: 59746-127-10
Package Description: 1000 TABLET in 1 BOTTLE (59746-127-10)

NDC Information of Hydrochlorothiazide

NDC Code 59746-127-10
Proprietary Name Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (59746-127-10)
Product NDC 59746-127
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071026
Marketing Category Name ANDA
Labeler Name JUBILANT CADISTA 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


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