Home > National Drug Code (NDC) > Hydrochlorothiazide

Hydrochlorothiazide - 0143-1256-51 - (Hydrochlorothiazide)

Alphabetical Index


Drug Information of Hydrochlorothiazide

Product NDC: 0143-1256
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: 0143-1256
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084878
Marketing Category: ANDA
Start Marketing Date: 20060801

Package Information of Hydrochlorothiazide

Package NDC: 0143-1256-51
Package Description: 5000 TABLET in 1 BOTTLE (0143-1256-51)

NDC Information of Hydrochlorothiazide

NDC Code 0143-1256-51
Proprietary Name Hydrochlorothiazide
Package Description 5000 TABLET in 1 BOTTLE (0143-1256-51)
Product NDC 0143-1256
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060801
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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


General Information