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Hydrochlorothiazide - 60505-2641-0 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 60505-2641
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: 60505-2641
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: 60505-2641-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2641-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Hydrochlorothiazide

NDC Code 60505-2641-0
Proprietary Name Hydrochlorothiazide
Package Description 10 BLISTER PACK in 1 CARTON (60505-2641-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 60505-2641
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 50
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Hydrochlorothiazide


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