Home > National Drug Code (NDC) > Hydroxyzine Hydrochloride

Hydroxyzine Hydrochloride - 60429-223-10 - (Hydroxyzine)

Alphabetical Index


Drug Information of Hydroxyzine Hydrochloride

Product NDC: 60429-223
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine
Active Ingredient(s): 10    mg/1 & nbsp;   Hydroxyzine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 60429-223
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040808
Marketing Category: ANDA
Start Marketing Date: 20080924

Package Information of Hydroxyzine Hydrochloride

Package NDC: 60429-223-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (60429-223-10)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 60429-223-10
Proprietary Name Hydroxyzine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (60429-223-10)
Product NDC 60429-223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080924
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


General Information