NDC 35561-346 – Fenofibrate

Fenofibrate 134 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC35561-346

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bostal LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207805
Marketed since
November 17, 2017
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 (3)

Package NDCDescriptionSince
35561-346-1190 CAPSULE in 1 BOTTLE (35561-346-11)Nov 17, 2017
35561-346-12100 CAPSULE in 1 BOTTLE (35561-346-12)Nov 20, 2020
35561-346-13500 CAPSULE in 1 BOTTLE (35561-346-13)Nov 20, 2020

Other Fenofibrate products