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Up and Up Childrens allergy medication - 11673-379-26 - (Diphenhydramine Hydrochloride)

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Drug Information of Up and Up Childrens allergy medication

Product NDC: 11673-379
Proprietary Name: Up and Up Childrens allergy medication
Non Proprietary Name: Diphenhydramine Hydrochloride
Active Ingredient(s): 12.5    mg/5mL & nbsp;   Diphenhydramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up Childrens allergy medication

Product NDC: 11673-379
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090708

Package Information of Up and Up Childrens allergy medication

Package NDC: 11673-379-26
Package Description: 1 BOTTLE in 1 CARTON (11673-379-26) > 118 mL in 1 BOTTLE

NDC Information of Up and Up Childrens allergy medication

NDC Code 11673-379-26
Proprietary Name Up and Up Childrens allergy medication
Package Description 1 BOTTLE in 1 CARTON (11673-379-26) > 118 mL in 1 BOTTLE
Product NDC 11673-379
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090708
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Up and Up Childrens allergy medication


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