NDC 63304-443 – Fenofibrate

Fenofibrate 43 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC63304-443

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA201748
Marketed since
March 2, 2015
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 (2)

Package NDCDescriptionSince
63304-443-05500 CAPSULE in 1 BOTTLE (63304-443-05)Mar 2, 2015
63304-443-3030 CAPSULE in 1 BOTTLE (63304-443-30)Mar 2, 2015

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