FDA.reportPublic FDA data

Application 011287

Type
NDA
Sponsor
CONCORDIA

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001KAYEXALATESODIUM POLYSTYRENE SULFONATEPOWDER;ORAL, RECTAL453.6GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
49186SUPPL2017-08-02
49156SUPPL2017-07-31
11928SUPPL2011-01-05
33038SUPPL2011-01-03
11927SUPPL2009-11-19
10759SUPPL2009-10-01
33037SUPPL2009-05-13
259SUPPL2009-05-04
258SUPPL2003-12-11
257SUPPL2003-06-08