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Hydroxyzine Hydrochloride - 0093-5061-05 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 0093-5061
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: 0093-5061
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088618
Marketing Category: ANDA
Start Marketing Date: 20121009

Package Information of Hydroxyzine Hydrochloride

Package NDC: 0093-5061-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-5061-05)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 0093-5061-05
Proprietary Name Hydroxyzine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0093-5061-05)
Product NDC 0093-5061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121009
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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