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Hydroxyzine Hydrochloride - 35356-942-60 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 35356-942
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: 35356-942
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040787
Marketing Category: ANDA
Start Marketing Date: 20120724

Package Information of Hydroxyzine Hydrochloride

Package NDC: 35356-942-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (35356-942-60)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 35356-942-60
Proprietary Name Hydroxyzine Hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (35356-942-60)
Product NDC 35356-942
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120724
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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