FDA.reportPublic FDA data

Application 065491

Type
ANDA
Sponsor
TEVA PHARMS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETILCAPSULE;ORAL250MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA,ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7334Mycophenolate MofetilMycophenolate MofetilTeva Pharmaceuticals USA, Inc.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
24045ORIG2015-07-02
44244ORIG2009-07-15