NDC 68180-232 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68180-232

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204019
Marketed since
July 1, 2020
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
68180-232-0990 TABLET in 1 BOTTLE (68180-232-09)Jul 1, 2020

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