Orange Book product · Generic (ANDA)
PHENYLBUTAZONE
PHENYLBUTAZONE
At a glance
Jun 16, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 16, 1982
44 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
PHENYLBUTAZONE
Strength
100MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 087774
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PHENYLBUTAZONE
- —BUTAZOLIDINBrand (NDA)
NDA 008319 · NOVARTIS
- 1985PHENYLBUTAZONEGeneric (ANDA)
ANDA 088994 · SUN PHARM INDUSTRIES
- 1985PHENYLBUTAZONEGeneric (ANDA)
ANDA 088863 · SUN PHARM INDUSTRIES
- 1983PHENYLBUTAZONEGeneric (ANDA)
ANDA 088218 · IVAX PHARMS
- 1982PHENYLBUTAZONEGeneric (ANDA)
ANDA 087756 · WATSON LABS
- 1982PHENYLBUTAZONEGeneric (ANDA)
ANDA 087674 · WATSON LABS
- —AZOLIDGeneric (ANDA)
ANDA 087260 · SANOFI AVENTIS US
- —AZOLIDGeneric (ANDA)
ANDA 087091 · SANOFI AVENTIS US
- —PHENYLBUTAZONEGeneric (ANDA)
ANDA 084339 · FOSUN PHARMA
- —PHENYLBUTAZONEGeneric (ANDA)
ANDA 086151 · 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.
