Orange Book product · Generic (ANDA)
MYCOPHENOLATE MOFETIL
MYCOPHENOLATE MOFETIL
At a glance
Jul 29, 2021
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 29, 2021
5 yr ago
Today
Pharmaceutical detail
Active ingredient
MYCOPHENOLATE MOFETIL
Strength
200MG/ML
Dosage form
FOR SUSPENSION
Route
ORAL
TE code
AB
Application
ANDA 214525
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of MYCOPHENOLATE MOFETIL
- 2024MYHIBBINBrand (NDA)
NDA 216482 · AZURITY
- 1998CELLCEPTBrand (NDA)
NDA 050759 · ROCHE PALO
- 1997CELLCEPTBrand (NDA)
NDA 050723 · ROCHE PALO
- 1995CELLCEPTBrand (NDA)
NDA 050722 · ROCHE PALO
- 2026MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 218566 · CONCORD BIOTECH LTD
- 2024MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 214079 · WUXI
- 2024MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 207022 · HETERO LABS LTD V
- 2024MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 208119 · HETERO LABS LTD V
- 2024MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 218227 · AUROBINDO PHARMA LTD
- 2024MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 217937 · AUROBINDO PHARMA
- 2024MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 217828 · AUROBINDO PHARMA LTD
- 2023MYCOPHENOLATE MOFETILGeneric (ANDA)
ANDA 213955 · RISING
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

