NDC 13668-440 – Fenofibrate

Fenofibrate 67 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC13668-440

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Torrent Pharmaceuticals Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210782
Marketed since
July 1, 2018
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 (3)

Package NDCDescriptionSince
13668-440-01100 CAPSULE in 1 BOTTLE (13668-440-01)Jul 1, 2018
13668-440-05500 CAPSULE in 1 BOTTLE (13668-440-05)Jul 1, 2018
13668-440-9090 CAPSULE in 1 BOTTLE (13668-440-90)Jul 1, 2018

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