Orange Book product · Generic (ANDA)
SULFINPYRAZONE
SULFINPYRAZONE
At a glance
Feb 17, 1984
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 17, 1984
42 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
SULFINPYRAZONE
Strength
200MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 088666
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SULFINPYRAZONE
- —ANTURANEBrand (NDA)
NDA 011556 · NOVARTIS
- 1985SULFINPYRAZONEGeneric (ANDA)
ANDA 088934 · PAR PHARM
- 1985SULFINPYRAZONEGeneric (ANDA)
ANDA 088933 · PAR PHARM
- 1982SULFINPYRAZONEGeneric (ANDA)
ANDA 087770 · IVAX PHARMS
- 1982SULFINPYRAZONEGeneric (ANDA)
ANDA 087666 · BARR
- 1982SULFINPYRAZONEGeneric (ANDA)
ANDA 087665 · BARR
- 1982SULFINPYRAZONEGeneric (ANDA)
ANDA 087769 · IVAX PHARMS
- 1982SULFINPYRAZONEGeneric (ANDA)
ANDA 087667 · 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.
