Orange Book product · Brand (NDA)
DAYPRO
OXAPROZIN
At a glance
Oct 29, 1992
Approved
Brand (NDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 29, 1992
34 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
OXAPROZIN
Strength
600MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
NDA 018841
Product number
004
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
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.
- 2023COXANTOBrand (NDA)
NDA 217927 · SOLUBIOMIX
- 2017OXAPROZINGeneric (ANDA)
ANDA 208633 · AMNEAL PHARMS CO
- 2004OXAPROZINGeneric (ANDA)
ANDA 075987 · CHARTWELL
- 2002OXAPROZINGeneric (ANDA)
ANDA 075849 · TEVA
- 2002OXAPROZINGeneric (ANDA)
ANDA 075846 · IVAX SUB TEVA PHARMS
- 2002OXAPROZINGeneric (ANDA)
ANDA 075844 · SUN PHARM INDS INC
- 2001OXAPROZINGeneric (ANDA)
ANDA 075843 · ACTAVIS ELIZABETH
- 2001OXAPROZINGeneric (ANDA)
ANDA 075851 · PHARMOBEDIENT
- 2001OXAPROZINGeneric (ANDA)
ANDA 075850 · SANDOZ
- 2001OXAPROZINGeneric (ANDA)
ANDA 075842 · AARXION ANDA HLDING
- 2001OXAPROZINGeneric (ANDA)
ANDA 075847 · MYLAN PHARMS INC
- 2001OXAPROZINGeneric (ANDA)
ANDA 075848 · WATSON LABS
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.
