Home > National Drug Code (NDC) > Hydrochlorothiazide

Hydrochlorothiazide - 55154-0833-9 - (Hydrochlorothiazide)

Alphabetical Index


Drug Information of Hydrochlorothiazide

Product NDC: 55154-0833
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: 55154-0833
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040412
Marketing Category: ANDA
Start Marketing Date: 20110506

Package Information of Hydrochlorothiazide

Package NDC: 55154-0833-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-0833-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Hydrochlorothiazide

NDC Code 55154-0833-9
Proprietary Name Hydrochlorothiazide
Package Description 6 BLISTER PACK in 1 CARTON (55154-0833-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-0833
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110506
Marketing Category Name ANDA
Labeler Name Cardinal Health
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