NDC 33342-340 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC33342-340

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210248
Marketed since
November 13, 2024
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (4)

Package NDCDescriptionSince
33342-340-0730 TABLET in 1 BOTTLE (33342-340-07)Nov 13, 2024
33342-340-1090 TABLET in 1 BOTTLE (33342-340-10)Nov 13, 2024
33342-340-1210 BLISTER PACK in 1 CARTON (33342-340-12) / 10 TABLET in 1 BLISTER PACKNov 13, 2024
33342-340-15500 TABLET in 1 BOTTLE (33342-340-15)Nov 13, 2024

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