NDC 27241-118 – Fenofibrate

Fenofibrate 67 mg/1 · Capsule · Oral

Human Prescription Drug 2 recalls

Product NDC27241-118

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Ajanta Pharma USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210705
Marketed since
September 10, 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 (2)

Package NDCDescriptionSince
27241-118-04100 CAPSULE in 1 BOTTLE (27241-118-04)Sep 10, 2018
27241-118-05500 CAPSULE in 1 BOTTLE (27241-118-05)Aug 1, 2019

Recalls mentioning this NDC

Other Fenofibrate products