NDC 69097-895 – Fenofibrate

Fenofibrate 134 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC69097-895

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Cipla USA Inc.,
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207378
Marketed since
March 30, 2017
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
69097-895-0230 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-02)Mar 30, 2017
69097-895-07100 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-07)Mar 30, 2017
69097-895-12500 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-12)Mar 30, 2017

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