Orange Book product · Generic (ANDA)
RILUZOLE
RILUZOLE
At a glance
Jan 29, 2003
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 29, 2003
23 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
RILUZOLE
Strength
50MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 076173
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of RILUZOLE
- 2019EXSERVANBrand (NDA)
NDA 212640 · AQUESTIVE
- 2018TIGLUTIK KITBrand (NDA)
NDA 209080 · ITALFARMACO SA
- 1995RILUTEKBrand (NDA)
NDA 020599 · AZURITY
- 2024RILUZOLEGeneric (ANDA)
ANDA 216035 · ALKEM LABS LTD
- 2019RILUZOLEGeneric (ANDA)
ANDA 206045 · KENTON
- 2018RILUZOLEGeneric (ANDA)
ANDA 204430 · DAITO PHARMS CO LTD
- 2016RILUZOLEGeneric (ANDA)
ANDA 204048 · ALKEM LABS LTD
- 2013RILUZOLEGeneric (ANDA)
ANDA 203042 · PHARMOBEDIENT
- 2013RILUZOLEGeneric (ANDA)
ANDA 091300 · APOTEX CORP
- 2013RILUZOLEGeneric (ANDA)
ANDA 091394 · GLENMARK PHARMS LTD
- 2013RILUZOLEGeneric (ANDA)
ANDA 091417 · SUN PHARM INDS 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.
