NDC 46708-361 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC46708-361

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210476
Marketed since
August 9, 2019
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
46708-361-3030 TABLET, FILM COATED in 1 BOTTLE (46708-361-30)Aug 9, 2019
46708-361-71500 TABLET, FILM COATED in 1 BOTTLE (46708-361-71)Aug 9, 2019
46708-361-9090 TABLET, FILM COATED in 1 BOTTLE (46708-361-90)Aug 9, 2019

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