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Hydrochlorothiazide - 63629-1413-3 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 63629-1413
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: 63629-1413
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040807
Marketing Category: ANDA
Start Marketing Date: 20100820

Package Information of Hydrochlorothiazide

Package NDC: 63629-1413-3
Package Description: 90 TABLET in 1 BOTTLE (63629-1413-3)

NDC Information of Hydrochlorothiazide

NDC Code 63629-1413-3
Proprietary Name Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (63629-1413-3)
Product NDC 63629-1413
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100820
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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