Orange Book product · Brand (NDA)
AEROSPAN HFA
FLUNISOLIDE
At a glance
Jan 27, 2006
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 27, 2006
20 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
FLUNISOLIDE
Strength
0.078MG/INH
Dosage form
AEROSOL, METERED
Route
INHALATION
TE code
Not listed
Application
NDA 021247
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.
- 1995NASARELBrand (NDA)
NDA 020409 · TEVA BRANDED PHARM
- 1984AEROBIDBrand (NDA)
NDA 018340 · ROCHE PALO
- —NASALIDEBrand (NDA)
NDA 018148 · IVAX RES
- 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.
