Orange Book product · Generic (ANDA)
FENOFIBRATE (MICRONIZED)
FENOFIBRATE
At a glance
Oct 31, 2014
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 31, 2014
11 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
FENOFIBRATE
Strength
43MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 201748
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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- 2021FENOFIBRATE (MICRONIZED)Generic (ANDA)
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- 2021FENOFIBRATEGeneric (ANDA)
ANDA 208476 · BOSTAL
- 2020FENOFIBRATE (MICRONIZED)Generic (ANDA)
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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.
