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Hydrochlorothiazide - 21695-537-30 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 21695-537
Proprietary Name: Hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 12.5    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrochlorothiazide

Product NDC: 21695-537
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040707
Marketing Category: ANDA
Start Marketing Date: 20070227

Package Information of Hydrochlorothiazide

Package NDC: 21695-537-30
Package Description: 30 TABLET in 1 BOTTLE (21695-537-30)

NDC Information of Hydrochlorothiazide

NDC Code 21695-537-30
Proprietary Name Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE (21695-537-30)
Product NDC 21695-537
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070227
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Hydrochlorothiazide


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