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Hydroxyzine Hydrochloride - 54868-2032-0 - (hydroxyzine hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 54868-2032
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: hydroxyzine hydrochloride
Active Ingredient(s): 10    mg/5mL & nbsp;   hydroxyzine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 54868-2032
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040010
Marketing Category: ANDA
Start Marketing Date: 19940801

Package Information of Hydroxyzine Hydrochloride

Package NDC: 54868-2032-0
Package Description: 473 mL in 1 BOTTLE, PLASTIC (54868-2032-0)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 54868-2032-0
Proprietary Name Hydroxyzine Hydrochloride
Package Description 473 mL in 1 BOTTLE, PLASTIC (54868-2032-0)
Product NDC 54868-2032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydroxyzine hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19940801
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/5mL
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


General Information