NDC 68071-2369 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68071-2369

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA205118
Marketed since
May 5, 2016
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (1)

Package NDCDescriptionSince
68071-2369-990 TABLET, COATED in 1 BOTTLE (68071-2369-9)Mar 17, 2021

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