NDC 60505-3121 – Fenofibrate

Fenofibrate 130 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC60505-3121

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Apotex Corp.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202252
Marketed since
July 26, 2013
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (4)

Package NDCDescriptionSince
60505-3121-1100 CAPSULE in 1 BOTTLE (60505-3121-1)Jul 26, 2013
60505-3121-330 CAPSULE in 1 BOTTLE (60505-3121-3)Jul 26, 2013
60505-3121-5500 CAPSULE in 1 BOTTLE (60505-3121-5)Jul 26, 2013
60505-3121-990 CAPSULE in 1 BOTTLE (60505-3121-9)Jul 26, 2013

Other Fenofibrate products