NDC 62332-086 – Fenofibrate

Fenofibrate 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC62332-086

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA213842
Marketed since
October 22, 2020
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 (3)

Package NDCDescriptionSince
62332-086-3030 CAPSULE in 1 BOTTLE (62332-086-30)Oct 22, 2020
62332-086-31100 CAPSULE in 1 BOTTLE (62332-086-31)Oct 22, 2020
62332-086-71500 CAPSULE in 1 BOTTLE (62332-086-71)Oct 22, 2020

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