Orange Book product · Brand (NDA)
PARAFON FORTE DSC
CHLORZOXAZONE
At a glance
Jun 15, 1987
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 15, 1987
39 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
CHLORZOXAZONE
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 011529
Product number
002
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.
- —PARAFLEXBrand (NDA)
NDA 011300 · ORTHO MCNEIL PHARM
- 2024CHLORZOXAZONEGeneric (ANDA)
ANDA 210961 · SENORES PHARMS
- 2023CHLORZOXAZONEGeneric (ANDA)
ANDA 089853 · AUROBINDO PHARMA LTD
- 2023CHLORZOXAZONEGeneric (ANDA)
ANDA 216925 · RISING
- 2023CHLORZOXAZONEGeneric (ANDA)
ANDA 214365 · ACME LABS
- 2023CHLORZOXAZONEGeneric (ANDA)
ANDA 214702 · COREPHARMA
- 2023CHLORZOXAZONEGeneric (ANDA)
ANDA 212047 · SOMERSET THERAPS LLC
- 2023CHLORZOXAZONEGeneric (ANDA)
ANDA 215540 · AJENAT PHARMS
- 2022CHLORZOXAZONEGeneric (ANDA)
ANDA 214941 · COREPHARMA
- 2022CHLORZOXAZONEGeneric (ANDA)
ANDA 213126 · RISING
- 2021CHLORZOXAZONEGeneric (ANDA)
ANDA 215158 · SENORES PHARMS
- 2021CHLORZOXAZONEGeneric (ANDA)
ANDA 212743 · PH HEALTH
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.
