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Hydroxyzine - 0904-0358-60 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine

Product NDC: 0904-0358
Proprietary Name: Hydroxyzine
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

Product NDC: 0904-0358
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040787
Marketing Category: ANDA
Start Marketing Date: 20070320

Package Information of Hydroxyzine

Package NDC: 0904-0358-60
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0904-0358-60)

NDC Information of Hydroxyzine

NDC Code 0904-0358-60
Proprietary Name Hydroxyzine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0904-0358-60)
Product NDC 0904-0358
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070320
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine


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