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Hydroxyzine Hydrochloride - 49999-035-30 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 49999-035
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: 49999-035
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091176
Marketing Category: ANDA
Start Marketing Date: 20111128

Package Information of Hydroxyzine Hydrochloride

Package NDC: 49999-035-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (49999-035-30)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 49999-035-30
Proprietary Name Hydroxyzine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (49999-035-30)
Product NDC 49999-035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111128
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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