Home > National Drug Code (NDC) > Hydroxyzine Hydrochloride

Hydroxyzine Hydrochloride - 10702-011-01 - (Hydroxyzine Hydrochloride)

Alphabetical Index


Drug Information of Hydroxyzine Hydrochloride

Product NDC: 10702-011
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Hydroxyzine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 10702-011
Labeler Name: KVK-Tech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040787
Marketing Category: ANDA
Start Marketing Date: 20120724

Package Information of Hydroxyzine Hydrochloride

Package NDC: 10702-011-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (10702-011-01)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 10702-011-01
Proprietary Name Hydroxyzine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (10702-011-01)
Product NDC 10702-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120724
Marketing Category Name ANDA
Labeler Name KVK-Tech, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


General Information