Application 204043

Type
ANDA
Sponsor
AKORN INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001MYCOPHENOLATE MOFETIL HYDROCHLORIDEMYCOPHENOLATE MOFETIL HYDROCHLORIDEINJECTABLE;INJECTION500MG/VIALNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
17478-422Mycophenolate MofetilMycophenolate MofetilAkornANDACurrent
17478-422Mycophenolate MofetilMycophenolate MofetilAkorn, Inc.ANDACurrent
17478-422Mycophenolate MofetilMycophenolate MofetilAkorn, Inc.ANDACurrent
17478-422Mycophenolate MofetilMycophenolate MofetilAkorn, Inc.ANDACurrent
17478-422Mycophenolate MofetilMycophenolate MofetilAkornANDACurrent
17478-422Mycophenolate MofetilMycophenolate MofetilAkornANDACurrent
17478-957Mycophenolate MofetilMycophenolate MofetilAkorn, Inc.ANDACurrent
17478-957Mycophenolate MofetilMycophenolate MofetilAkornANDACurrent
17478-957Mycophenolate MofetilMycophenolate MofetilAkorn, Inc.ANDACurrent
17478-957Mycophenolate MofetilMycophenolate MofetilAkornANDACurrent
17478-957Mycophenolate MofetilMycophenolate MofetilAkorn, Inc.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
76490ORIG 2023-11-07
47444ORIG2017-03-03