NDC 46708-245 – Fenofibric Acid

Fenofibric Acid 135 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC46708-245

Product details

Brand name
Fenofibric Acid
Generic name
Fenofibric Acid
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208705
Marketed since
May 18, 2017
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibric acid →

Package NDC codes (3)

Package NDCDescriptionSince
46708-245-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-245-30)May 18, 2017
46708-245-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-245-90)May 18, 2017
46708-245-911000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-245-91)May 18, 2017

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