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HydrOXYzine Hydrochloride - 16714-083-04 - (HydrOXYzine Hydrochloride)

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Drug Information of HydrOXYzine Hydrochloride

Product NDC: 16714-083
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: 16714-083
Labeler Name: Northstar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040840
Marketing Category: ANDA
Start Marketing Date: 20091111

Package Information of HydrOXYzine Hydrochloride

Package NDC: 16714-083-04
Package Description: 100 TABLET in 1 BOTTLE (16714-083-04)

NDC Information of HydrOXYzine Hydrochloride

NDC Code 16714-083-04
Proprietary Name HydrOXYzine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (16714-083-04)
Product NDC 16714-083
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HydrOXYzine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091111
Marketing Category Name ANDA
Labeler Name Northstar RxLLC
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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