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Up and Up childrens ibuprofen - 11673-166-28 - (Ibuprofen)

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Drug Information of Up and Up childrens ibuprofen

Product NDC: 11673-166
Proprietary Name: Up and Up childrens ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up childrens ibuprofen

Product NDC: 11673-166
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 20090612

Package Information of Up and Up childrens ibuprofen

Package NDC: 11673-166-28
Package Description: 1 BOTTLE in 1 CARTON (11673-166-28) > 148 mL in 1 BOTTLE

NDC Information of Up and Up childrens ibuprofen

NDC Code 11673-166-28
Proprietary Name Up and Up childrens ibuprofen
Package Description 1 BOTTLE in 1 CARTON (11673-166-28) > 148 mL in 1 BOTTLE
Product NDC 11673-166
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Up and Up childrens ibuprofen


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