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Hydrochlorothiazide - 63739-128-10 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 63739-128
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: 63739-128
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040412
Marketing Category: ANDA
Start Marketing Date: 20070628

Package Information of Hydrochlorothiazide

Package NDC: 63739-128-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-128-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Hydrochlorothiazide

NDC Code 63739-128-10
Proprietary Name Hydrochlorothiazide
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-128-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-128
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070628
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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