Orange Book product · Brand (NDA)
NASALIDE
FLUNISOLIDE
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
FLUNISOLIDE
Strength
0.025MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
SPRAY, METERED
Route
NASAL
TE code
Not listed
Application
NDA 018148
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 2006AEROSPAN HFABrand (NDA)
NDA 021247 · PHARMOBEDIENT
- 1995NASARELBrand (NDA)
NDA 020409 · TEVA BRANDED PHARM
- 1984AEROBIDBrand (NDA)
NDA 018340 · ROCHE PALO
- 2022FLUNISOLIDEGeneric (ANDA)
ANDA 207802 · RICONPHARMA LLC
- 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.
