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Up and Up infants acetaminophen - 11673-289-10 - (Acetaminophen)

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Drug Information of Up and Up infants acetaminophen

Product NDC: 11673-289
Proprietary Name: Up and Up infants acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 80    mg/.8mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up infants acetaminophen

Product NDC: 11673-289
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090612

Package Information of Up and Up infants acetaminophen

Package NDC: 11673-289-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (11673-289-10) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of Up and Up infants acetaminophen

NDC Code 11673-289-10
Proprietary Name Up and Up infants acetaminophen
Package Description 1 BOTTLE, DROPPER in 1 CARTON (11673-289-10) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 11673-289
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Target Corporation
Substance Name ACETAMINOPHEN
Strength Number 80
Strength Unit mg/.8mL
Pharmaceutical Classes

Complete Information of Up and Up infants acetaminophen


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