Orange Book product · Generic (ANDA)
CHOLEDYL SA
OXTRIPHYLLINE
At a glance
May 24, 1983
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 24, 1983
43 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
OXTRIPHYLLINE
Strength
400MG
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
ANDA 087863
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 087866 · WATSON LABS
- 1983OXTRIPHYLLINEGeneric (ANDA)
ANDA 087835 · WATSON LABS
- —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.
