Application 050547

Type
NDA
Sponsor
US PHARM HOLDINGS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001CLAFORANCEFOTAXIME SODIUMINJECTABLE;INJECTIONEQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
002CLAFORANCEFOTAXIME SODIUMINJECTABLE;INJECTIONEQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
003CLAFORANCEFOTAXIME SODIUMINJECTABLE;INJECTIONEQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
004CLAFORANCEFOTAXIME SODIUMINJECTABLE;INJECTIONEQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
38974SUPPL2015-04-14
7809SUPPL2015-03-24
30076SUPPL2014-02-25
17868SUPPL2014-02-25
17867SUPPL2011-09-16
7808SUPPL2011-09-13
30075SUPPL2009-06-02
17866SUPPL2008-02-25
7807SUPPL2008-02-25
7806SUPPL2004-09-03
7805SUPPL2004-06-24
30074SUPPL2002-01-18