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up and up childrens acetaminophen - 11673-759-26 - (Acetaminophen)

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Drug Information of up and up childrens acetaminophen

Product NDC: 11673-759
Proprietary Name: up and up childrens acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 160    mg/5mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of up and up childrens acetaminophen

Product NDC: 11673-759
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110716

Package Information of up and up childrens acetaminophen

Package NDC: 11673-759-26
Package Description: 1 BOTTLE in 1 CARTON (11673-759-26) > 118 mL in 1 BOTTLE

NDC Information of up and up childrens acetaminophen

NDC Code 11673-759-26
Proprietary Name up and up childrens acetaminophen
Package Description 1 BOTTLE in 1 CARTON (11673-759-26) > 118 mL in 1 BOTTLE
Product NDC 11673-759
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20110716
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Target Corporation
Substance Name ACETAMINOPHEN
Strength Number 160
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of up and up childrens acetaminophen


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