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Hydrochlorothiazide - 68788-9090-8 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 68788-9090
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: 68788-9090
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040807
Marketing Category: ANDA
Start Marketing Date: 20110103

Package Information of Hydrochlorothiazide

Package NDC: 68788-9090-8
Package Description: 120 TABLET in 1 BOTTLE, DISPENSING (68788-9090-8)

NDC Information of Hydrochlorothiazide

NDC Code 68788-9090-8
Proprietary Name Hydrochlorothiazide
Package Description 120 TABLET in 1 BOTTLE, DISPENSING (68788-9090-8)
Product NDC 68788-9090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110103
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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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