Orange Book product · Generic (ANDA)
FENOFIBRATE
FENOFIBRATE
At a glance
Oct 31, 2005
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 31, 2005
20 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
FENOFIBRATE
Strength
54MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 076635
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FENOFIBRATE
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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.
