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Hydroxyzine Hydrochloride - 55154-5377-0 - (hydroxyzine hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 55154-5377
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: 55154-5377
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091176
Marketing Category: ANDA
Start Marketing Date: 20100723

Package Information of Hydroxyzine Hydrochloride

Package NDC: 55154-5377-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5377-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Hydroxyzine Hydrochloride

NDC Code 55154-5377-0
Proprietary Name Hydroxyzine Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-5377-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydroxyzine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100723
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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