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Hydroxyzine - 0615-1525-39 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine

Product NDC: 0615-1525
Proprietary Name: Hydroxyzine
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

Product NDC: 0615-1525
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040786
Marketing Category: ANDA
Start Marketing Date: 20070320

Package Information of Hydroxyzine

Package NDC: 0615-1525-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-1525-39)

NDC Information of Hydroxyzine

NDC Code 0615-1525-39
Proprietary Name Hydroxyzine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-1525-39)
Product NDC 0615-1525
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 NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine


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