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Hydroxyzine Hydrochloride - 50111-307-02 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 50111-307
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 10    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: 50111-307
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088617
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Hydroxyzine Hydrochloride

Package NDC: 50111-307-02
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (50111-307-02)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 50111-307-02
Proprietary Name Hydroxyzine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (50111-307-02)
Product NDC 50111-307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Pliva 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