Orange Book product · Brand (NDA)
FURACIN
NITROFURAZONE
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
NITROFURAZONE
Strength
0.2%
Dosage form
OINTMENT
Route
TOPICAL
TE code
Not listed
Application
NDA 005795
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- —ACTIN-NBrand (NDA)
NDA 017343 · SHERWOOD MEDCL
- —FURACINGeneric (ANDA)
ANDA 083789 · SHIRE
- —NITROFURAZONEGeneric (ANDA)
ANDA 086077 · AMBIX
- —NITROFURAZONEGeneric (ANDA)
ANDA 084393 · LANNETT
- —NITROFURAZONEGeneric (ANDA)
ANDA 084968 · PERRIGO NEW YORK
- —NITROFURAZONEGeneric (ANDA)
ANDA 086156 · SUN PHARMA CANADA
- —NITROFURAZONEGeneric (ANDA)
ANDA 086766 · WENDT
- —FURACINGeneric (ANDA)
ANDA 083791 · SHIRE
- —NITROFURAZONEGeneric (ANDA)
ANDA 085130 · PERRIGO NEW YORK
- —NITROFURAZONEGeneric (ANDA)
ANDA 087081 · WENDT
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.
