NDC 68180-130 – Fenofibrate

Fenofibrate 43 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68180-130

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021695
Marketed since
February 22, 2013
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
68180-130-0630 CAPSULE in 1 BOTTLE (68180-130-06)Feb 22, 2013

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