Application 210370

Type
ANDA
Sponsor
VISTAPHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETILSUSPENSION;ORAL200MG/MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, LLCANDACurrent
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, LLCANDACurrent
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, Inc.ANDACurrent
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, Inc.ANDACurrent
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, Inc.ANDACurrent
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, Inc.ANDACurrent
66689-307Mycophenolate MofetilMycophenolate MofetilVistaPharm, Inc.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
76494ORIG 2023-11-07