Orange Book product · Generic (ANDA)
OXTRIPHYLLINE
OXTRIPHYLLINE
At a glance
Aug 25, 1983
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 25, 1983
43 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
OXTRIPHYLLINE
Strength
100MG
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
TE code
Not listed
Application
ANDA 087866
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of OXTRIPHYLLINE
- 1984CHOLEDYLBrand (NDA)
NDA 009268 · PARKE DAVIS
- 1983OXTRIPHYLLINEGeneric (ANDA)
ANDA 088243 · MORTON GROVE
- 1983OXTRIPHYLLINE PEDIATRICGeneric (ANDA)
ANDA 088242 · MORTON GROVE
- 1983OXTRIPHYLLINEGeneric (ANDA)
ANDA 087835 · WATSON LABS
- 1983CHOLEDYL SAGeneric (ANDA)
ANDA 087863 · WARNER CHILCOTT LLC
- —CHOLEDYL SAGeneric (ANDA)
ANDA 086742 · WARNER CHILCOTT LLC
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.
