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Hydrochlorothiazide - 60505-2640-8 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 60505-2640
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: 60505-2640
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040774
Marketing Category: ANDA
Start Marketing Date: 20080129

Package Information of Hydrochlorothiazide

Package NDC: 60505-2640-8
Package Description: 1000 TABLET in 1 BOTTLE (60505-2640-8)

NDC Information of Hydrochlorothiazide

NDC Code 60505-2640-8
Proprietary Name Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (60505-2640-8)
Product NDC 60505-2640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080129
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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


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