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Hydrochlorothiazide - 0527-1414-01 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 0527-1414
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: 0527-1414
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084324
Marketing Category: ANDA
Start Marketing Date: 20070501

Package Information of Hydrochlorothiazide

Package NDC: 0527-1414-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0527-1414-01)

NDC Information of Hydrochlorothiazide

NDC Code 0527-1414-01
Proprietary Name Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0527-1414-01)
Product NDC 0527-1414
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070501
Marketing Category Name ANDA
Labeler Name Lannett Company, 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


General Information