Orange Book product · Brand (NDA)
CHOLEDYL
OXTRIPHYLLINE
At a glance
Nov 27, 1984
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 27, 1984
42 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
OXTRIPHYLLINE
Strength
100MG/5ML
Dosage form
SOLUTION
Route
ORAL
TE code
Not listed
Application
NDA 009268
Product number
012
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 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
- 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.
