NDC 50268-338 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50268-338

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090856
Marketed since
September 22, 2022
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 (1)

Package NDCDescriptionSince
50268-338-1220 BLISTER PACK in 1 BOX (50268-338-12) / 1 TABLET in 1 BLISTER PACK (50268-338-11)Sep 22, 2022

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