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HydrOXYzine Hydrochloride - 63739-483-10 - (HydrOXYzine Hydrochloride)

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Drug Information of HydrOXYzine Hydrochloride

Product NDC: 63739-483
Proprietary Name: HydrOXYzine Hydrochloride
Non Proprietary Name: HydrOXYzine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   HydrOXYzine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of HydrOXYzine Hydrochloride

Product NDC: 63739-483
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040841
Marketing Category: ANDA
Start Marketing Date: 20110301

Package Information of HydrOXYzine Hydrochloride

Package NDC: 63739-483-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-483-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of HydrOXYzine Hydrochloride

NDC Code 63739-483-10
Proprietary Name HydrOXYzine Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-483-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-483
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HydrOXYzine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110301
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of HydrOXYzine Hydrochloride


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