FDA.reportPublic FDA data

Application 202720

Type
ANDA
Sponsor
TEVA PHARMS USA

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001MYCOPHENOLIC ACIDMYCOPHENOLIC ACIDTABLET, DELAYED RELEASE;ORAL180MGNoNo
002MYCOPHENOLIC ACIDMYCOPHENOLIC ACIDTABLET, DELAYED RELEASE;ORAL360MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0093-7031Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7031Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7031Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7032Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7032Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7032Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-7032Mycophenolic AcidMycophenolic AcidTeva Pharmaceuticals USA, Inc.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
24103ORIG2015-07-06