TEVA PHARMS USA Application 211272

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	MYCOPHENOLATE MOFETIL	MYCOPHENOLATE MOFETIL	FOR SUSPENSION;ORAL	200MG/ML	No	No

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0480-1175	Mycophenolate Mofetil	Mycophenolate Mofetil	Teva Pharmaceuticals, Inc.	ANDA	Current
0480-1175	Mycophenolate Mofetil	Mycophenolate Mofetil	Teva Pharmaceuticals, Inc.	ANDA	Current

Document, Submission type, Date table
Document	Submission type	Date
76505	ORIG	2023-11-07