Orange Book product · Generic (ANDA)
FENOFIBRATE
FENOFIBRATE
At a glance
Dec 07, 2012
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 07, 2012
13 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
FENOFIBRATE
Strength
48MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 202856
Product number
001
Marketing status
RX
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.
