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Hydroxyzine Hydrochloride - 51079-806-20 - (hydroxyzine hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 51079-806
Proprietary Name: Hydroxyzine Hydrochloride
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 Hydrochloride

Product NDC: 51079-806
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091176
Marketing Category: ANDA
Start Marketing Date: 20100723

Package Information of Hydroxyzine Hydrochloride

Package NDC: 51079-806-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-806-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-806-01)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 51079-806-20
Proprietary Name Hydroxyzine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-806-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-806-01)
Product NDC 51079-806
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydroxyzine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100723
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


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