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Last Updated: August 5, 2020

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Details for New Drug Application (NDA): 075010

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Summary for 075010
Tradename:IBUPROFEN
Applicant:Lnk
Ingredient:ibuprofen
Patents:0
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 075010
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
IBUPROFEN ibuprofen TABLET;ORAL 075010 ANDA Walgreen Company 0363-0291 0363-0291-03 10 TABLET, FILM COATED in 1 BOTTLE (0363-0291-03)
IBUPROFEN ibuprofen TABLET;ORAL 075010 ANDA Walgreen Company 0363-0291 0363-0291-08 1 BOTTLE in 1 CARTON (0363-0291-08) > 24 TABLET, FILM COATED in 1 BOTTLE

Profile for product number 001

Active Rx/OTC/Discontinued:OTCDosage:TABLET;ORALStrength200MG
Approval Date:Mar 1, 1999TE:RLD:No

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