Application 017463

Type
NDA
Sponsor
MCNEIL CONSUMER

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
002MOTRINIBUPROFENTABLET;ORAL400MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
003MOTRINIBUPROFENTABLET;ORAL300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
004MOTRINIBUPROFENTABLET;ORAL600MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
005MOTRINIBUPROFENTABLET;ORAL800MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
23105ORIG2009-12-04
33275SUPPL2007-09-11
594SUPPL2007-09-11
13146SUPPL2006-01-30
10996SUPPL2006-01-25