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Hydroxyzine Hydrochloride - 0378-2587-10 - (hydroxyzine hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 0378-2587
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: 0378-2587
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091176
Marketing Category: ANDA
Start Marketing Date: 20120727

Package Information of Hydroxyzine Hydrochloride

Package NDC: 0378-2587-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2587-10)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 0378-2587-10
Proprietary Name Hydroxyzine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2587-10)
Product NDC 0378-2587
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydroxyzine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120727
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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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