Orange Book product · Generic (ANDA)
SULFISOXAZOLE
SULFISOXAZOLE
At a glance
Approved Prior to Jan 1, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
SULFISOXAZOLE
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 080189
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SULFISOXAZOLE
- —GANTRISINBrand (NDA)
NDA 006525 · ROCHE
- —SOSOLGeneric (ANDA)
ANDA 080036 · MK LABS
- —SOXAZOLEGeneric (ANDA)
ANDA 080366 · ALRA
- —SULFALARGeneric (ANDA)
ANDA 084955 · PARKE DAVIS
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 080142 · ANI PHARMS
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 084031 · BARR
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 080109 · IMPAX LABS
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 080085 · LANNETT
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 087649 · LEDERLE
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 084385 · PHARMERAL
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 080087 · PUREPAC PHARM
- —SULFISOXAZOLEGeneric (ANDA)
ANDA 085628 · RISING
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.
