NDC 60687-618 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-618

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090856
Marketed since
August 9, 2021
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
60687-618-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-618-21) / 1 TABLET in 1 BLISTER PACK (60687-618-11)Aug 9, 2021

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