NDC 68071-1712 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-1712

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211122
Marketed since
July 18, 2022
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
68071-1712-990 TABLET in 1 BOTTLE (68071-1712-9)Mar 1, 2023

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