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Hydroxyzine Hydrochloride - 63629-4929-2 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 63629-4929
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: 63629-4929
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040804
Marketing Category: ANDA
Start Marketing Date: 20080630

Package Information of Hydroxyzine Hydrochloride

Package NDC: 63629-4929-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (63629-4929-2)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 63629-4929-2
Proprietary Name Hydroxyzine Hydrochloride
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (63629-4929-2)
Product NDC 63629-4929
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080630
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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