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Hydroxyzine - 10544-210-20 - (Hydroxyzine)

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Drug Information of Hydroxyzine

Product NDC: 10544-210
Proprietary Name: Hydroxyzine
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

Product NDC: 10544-210
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088618
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Hydroxyzine

Package NDC: 10544-210-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (10544-210-20)

NDC Information of Hydroxyzine

NDC Code 10544-210-20
Proprietary Name Hydroxyzine
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (10544-210-20)
Product NDC 10544-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100517
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine


General Information