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up and up ibuprofen - 11673-685-26 - (Ibuprofen)

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Drug Information of up and up ibuprofen

Product NDC: 11673-685
Proprietary Name: up and up ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of up and up ibuprofen

Product NDC: 11673-685
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 20090710

Package Information of up and up ibuprofen

Package NDC: 11673-685-26
Package Description: 1 BOTTLE in 1 CARTON (11673-685-26) > 118 mL in 1 BOTTLE

NDC Information of up and up ibuprofen

NDC Code 11673-685-26
Proprietary Name up and up ibuprofen
Package Description 1 BOTTLE in 1 CARTON (11673-685-26) > 118 mL in 1 BOTTLE
Product NDC 11673-685
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090710
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 ibuprofen


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