Home > National Drug Code (NDC) > Hydrochlorothiazide

Hydrochlorothiazide - 42254-055-90 - (Hydrochlorothiazide)

Alphabetical Index


Drug Information of Hydrochlorothiazide

Product NDC: 42254-055
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: 42254-055
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040702
Marketing Category: ANDA
Start Marketing Date: 20100816

Package Information of Hydrochlorothiazide

Package NDC: 42254-055-90
Package Description: 90 TABLET in 1 BOTTLE (42254-055-90)

NDC Information of Hydrochlorothiazide

NDC Code 42254-055-90
Proprietary Name Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (42254-055-90)
Product NDC 42254-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100816
Marketing Category Name ANDA
Labeler Name Rebel Distributors 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