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Hydroxyzine Hydrochloride - 68788-9737-3 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 68788-9737
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 10    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: 68788-9737
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040786
Marketing Category: ANDA
Start Marketing Date: 20121008

Package Information of Hydroxyzine Hydrochloride

Package NDC: 68788-9737-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9737-3)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 68788-9737-3
Proprietary Name Hydroxyzine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68788-9737-3)
Product NDC 68788-9737
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121008
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


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