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Hydroxyzine Hydrochloride - 67405-671-96 - (Hydroxyzine)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 67405-671
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine
Active Ingredient(s): 25    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: 67405-671
Labeler Name: Harris Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040808
Marketing Category: ANDA
Start Marketing Date: 20070629

Package Information of Hydroxyzine Hydrochloride

Package NDC: 67405-671-96
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (67405-671-96)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 67405-671-96
Proprietary Name Hydroxyzine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (67405-671-96)
Product NDC 67405-671
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070629
Marketing Category Name ANDA
Labeler Name Harris Pharmaceutical, 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


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