Orange Book product · Generic (ANDA)
FLUNISOLIDE
FLUNISOLIDE
Generic (ANDA)ANDA 207802TE ABRX RICONPHARMA LLC
At a glance
Jun 16, 2022
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 16, 2022
4 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
FLUNISOLIDE
Strength
0.025MG/SPRAY
Dosage form
SPRAY, METERED
Route
NASAL
TE code
AB
Application
ANDA 207802
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FLUNISOLIDE
- 2006AEROSPAN HFABrand (NDA)
NDA 021247 · PHARMOBEDIENT
- 1995NASARELBrand (NDA)
NDA 020409 · TEVA BRANDED PHARM
- 1984AEROBIDBrand (NDA)
NDA 018340 · ROCHE PALO
- —NASALIDEBrand (NDA)
NDA 018148 · IVAX RES
- 2007FLUNISOLIDEGeneric (ANDA)
ANDA 077436 · APOTEX
- 2006FLUNISOLIDEGeneric (ANDA)
ANDA 077704 · RISING
- 2002FLUNISOLIDEGeneric (ANDA)
ANDA 074805 · BAUSCH
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.
