NDC 68788-7816 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7816

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213864
Marketed since
November 6, 2020
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 (2)

Package NDCDescriptionSince
68788-7816-330 TABLET in 1 BOTTLE (68788-7816-3)Nov 6, 2020
68788-7816-960 TABLET in 1 BOTTLE (68788-7816-9)Nov 6, 2020

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