NDC 33342-295 – Fenofibric acid

Choline Fenofibrate 135 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC33342-295

Product details

Brand name
Fenofibric acid
Generic name
Fenofibric acid
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA207796
Marketed since
February 26, 2024
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 (2)

Package NDCDescriptionSince
33342-295-1090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-295-10)Feb 26, 2024
33342-295-5610 BLISTER PACK in 1 CARTON (33342-295-56) / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACKFeb 26, 2024

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