NDC 65862-769 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC65862-769

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA205118
Marketed since
May 5, 2016
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 (5)

Package NDCDescriptionSince
65862-769-01100 TABLET, COATED in 1 BOTTLE (65862-769-01)May 5, 2016
65862-769-05500 TABLET, COATED in 1 BOTTLE (65862-769-05)May 5, 2016
65862-769-7810 BLISTER PACK in 1 CARTON (65862-769-78) / 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10)May 5, 2016
65862-769-9090 TABLET, COATED in 1 BOTTLE (65862-769-90)May 5, 2016
65862-769-991000 TABLET, COATED in 1 BOTTLE (65862-769-99)May 5, 2016

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