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Hydroxyzine Hydrochloride - 52125-356-02 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 52125-356
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 50    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: 52125-356
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088619
Marketing Category: ANDA
Start Marketing Date: 20130528

Package Information of Hydroxyzine Hydrochloride

Package NDC: 52125-356-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-356-02)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 52125-356-02
Proprietary Name Hydroxyzine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-356-02)
Product NDC 52125-356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130528
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


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