Orange Book product · Generic (ANDA)
FENOPROFEN CALCIUM
FENOPROFEN CALCIUM
At a glance
Jul 18, 2022
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 18, 2022
4 yr ago
Today
Pharmaceutical detail
Active ingredient
FENOPROFEN CALCIUM
Strength
EQ 400MG BASE
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 214475
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of FENOPROFEN CALCIUM
- —NALFONBrand (NDA)
NDA 017604 · PHARMACO
- —NALFONBrand (NDA)
NDA 017710 · DISTA
- 2023FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 215548 · MISEMER
- 1991FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072981 · WATSON LABS
- 1991FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072982 · WATSON LABS
- 1991FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072946 · WARNER CHILCOTT
- 1991FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072472 · WARNER CHILCOTT
- 1990FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072902 · SUN PHARM INDUSTRIES
- 1988FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072394 · RISING
- 1988FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072395 · RISING
- 1988FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072396 · RISING
- 1988FENOPROFEN CALCIUMGeneric (ANDA)
ANDA 072602 · 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.
