NDC 0904-7161 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0904-7161

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Major Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208709
Marketed since
December 15, 2016
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
0904-7161-61100 BLISTER PACK in 1 CARTON (0904-7161-61) / 1 TABLET in 1 BLISTER PACKDec 15, 2016

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