Orange Book product · Generic (ANDA)
APREMILAST
APREMILAST
At a glance
Nov 25, 2024
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 25, 2024
1 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
APREMILAST
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 211788
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of APREMILAST
- 2025OTEZLA XRBrand (NDA)
NDA 210745 · AMGEN INC
- 2014OTEZLABrand (NDA)
NDA 205437 · AMGEN INC
- 2025APREMILASTGeneric (ANDA)
ANDA 211834 · TORRENT
- 2024APREMILASTGeneric (ANDA)
ANDA 211887 · MSN
- 2024APREMILASTGeneric (ANDA)
ANDA 211734 · MANKIND PHARMA
- 2023APREMILASTGeneric (ANDA)
ANDA 211674 · GLENMARK PHARMS LTD
- 2023APREMILASTGeneric (ANDA)
ANDA 211878 · ANNORA
- 2023APREMILASTGeneric (ANDA)
ANDA 211716 · AUROBINDO PHARMA LTD
- 2023APREMILASTGeneric (ANDA)
ANDA 211756 · DR REDDYS
- 2023APREMILASTGeneric (ANDA)
ANDA 211774 · SHILPA
- 2022APREMILASTGeneric (ANDA)
ANDA 211897 · TEVA PHARMS USA INC
- 2021APREMILASTGeneric (ANDA)
ANDA 211761 · ALKEM LABS LTD
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.

