Orange Book product · Generic (ANDA)
TERIFLUNOMIDE
TERIFLUNOMIDE
At a glance
Feb 28, 2020
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 28, 2020
6 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
TERIFLUNOMIDE
Strength
7MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 209702
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of TERIFLUNOMIDE
- 2012AUBAGIOBrand (NDA)
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ANDA 209697 · TORRENT
- 2023TERIFLUNOMIDEGeneric (ANDA)
ANDA 209677 · SOLA PHARMS
- 2023TERIFLUNOMIDEGeneric (ANDA)
ANDA 209555 · NATCO
- 2023TERIFLUNOMIDEGeneric (ANDA)
ANDA 209639 · BIOCON PHARMA
- 2023TERIFLUNOMIDEGeneric (ANDA)
ANDA 209598 · HETERO LABS LTD V
- 2021TERIFLUNOMIDEGeneric (ANDA)
ANDA 209583 · BRECKENRIDGE
- 2019TERIFLUNOMIDEGeneric (ANDA)
ANDA 209623 · MSN
- 2019TERIFLUNOMIDEGeneric (ANDA)
ANDA 209572 · ALEMBIC
- 2019TERIFLUNOMIDEGeneric (ANDA)
ANDA 209690 · ACCORD HLTHCARE
- 2019TERIFLUNOMIDEGeneric (ANDA)
ANDA 209710 · SANDOZ
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.
