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Hydroxyzine Hydrochloride - 54569-1640-1 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 54569-1640
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): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 54569-1640
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087294
Marketing Category: ANDA
Start Marketing Date: 19950309

Package Information of Hydroxyzine Hydrochloride

Package NDC: 54569-1640-1
Package Description: 120 mL in 1 BOTTLE, PLASTIC (54569-1640-1)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 54569-1640-1
Proprietary Name Hydroxyzine Hydrochloride
Package Description 120 mL in 1 BOTTLE, PLASTIC (54569-1640-1)
Product NDC 54569-1640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 19950309
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/5mL
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


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