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HydrOXYzine hydrochloride - 57664-114-18 - (HydrOXYzine hydrochloride)

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Drug Information of HydrOXYzine hydrochloride

Product NDC: 57664-114
Proprietary Name: HydrOXYzine hydrochloride
Non Proprietary Name: HydrOXYzine hydrochloride
Active Ingredient(s): 50    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: 57664-114
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040899
Marketing Category: ANDA
Start Marketing Date: 20090331

Package Information of HydrOXYzine hydrochloride

Package NDC: 57664-114-18
Package Description: 1000 TABLET in 1 BOTTLE (57664-114-18)

NDC Information of HydrOXYzine hydrochloride

NDC Code 57664-114-18
Proprietary Name HydrOXYzine hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (57664-114-18)
Product NDC 57664-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HydrOXYzine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090331
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of HydrOXYzine hydrochloride


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