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up and up ibuprofen - 11673-183-83 - (Ibuprofen)

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Drug Information of up and up ibuprofen

Product NDC: 11673-183
Proprietary Name: up and up ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of up and up ibuprofen

Product NDC: 11673-183
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077349
Marketing Category: ANDA
Start Marketing Date: 20100311

Package Information of up and up ibuprofen

Package NDC: 11673-183-83
Package Description: 225 TABLET, FILM COATED in 1 BOTTLE (11673-183-83)

NDC Information of up and up ibuprofen

NDC Code 11673-183-83
Proprietary Name up and up ibuprofen
Package Description 225 TABLET, FILM COATED in 1 BOTTLE (11673-183-83)
Product NDC 11673-183
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100311
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up ibuprofen


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