NDC 68071-4991 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-4991

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210138
Marketed since
July 20, 2018
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
68071-4991-990 TABLET in 1 BOTTLE (68071-4991-9)Jul 26, 2019

Other Fenofibrate products