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Hydroxyzine Hydrochloride - 0517-4201-25 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 0517-4201
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 25    mg/mL & nbsp;   Hydroxyzine Hydrochloride
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 0517-4201
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087408
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Hydroxyzine Hydrochloride

Package NDC: 0517-4201-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4201-25) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Hydroxyzine Hydrochloride

NDC Code 0517-4201-25
Proprietary Name Hydroxyzine Hydrochloride
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4201-25) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-4201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


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