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Hydrochlorothiazide - 54868-0792-6 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 54868-0792
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: 54868-0792
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083177
Marketing Category: ANDA
Start Marketing Date: 19951004

Package Information of Hydrochlorothiazide

Package NDC: 54868-0792-6
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-0792-6)

NDC Information of Hydrochlorothiazide

NDC Code 54868-0792-6
Proprietary Name Hydrochlorothiazide
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-0792-6)
Product NDC 54868-0792
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19951004
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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