NDC 68071-5101 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-5101

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208709
Marketed since
December 15, 2016
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 (1)

Package NDCDescriptionSince
68071-5101-990 TABLET in 1 BOTTLE (68071-5101-9)Nov 4, 2019

Other Fenofibrate products