Orange Book product · Brand (NDA)
PSORCON
DIFLORASONE DIACETATE
At a glance
Nov 20, 1992
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 20, 1992
34 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
DIFLORASONE DIACETATE
Strength
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
CREAM
Route
TOPICAL
TE code
Not listed
Application
NDA 020205
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.
- 1985FLORONE EBrand (NDA)
NDA 019259 · PFIZER
- 1985PSORCONBrand (NDA)
NDA 019260 · PFIZER
- —FLORONEBrand (NDA)
NDA 017741 · PFIZER
- —PSORCON EBrand (NDA)
NDA 017994 · PFIZER
- 2018DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 210753 · THE J MOLNER
- 2017DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 207440 · RISING
- 2015DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 206572 · SCIEGEN PHARMS
- 2002DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 076263 · ANI PHARMS
- 2000DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 075508 · SUN PHARMA CANADA
- 1999DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 075331 · SUN PHARMA CANADA
- 1999DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 075374 · AVONDALE PHARMS
- 1998DIFLORASONE DIACETATEGeneric (ANDA)
ANDA 075187 · AVONDALE PHARMS
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.
