NDC 72319-017 – Everolimus

Everolimus 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72319-017

Product details

Brand name
Everolimus
Generic name
Everolimus
Labeler
i3 Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA219464
Marketed since
August 7, 2026
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor; mTOR Inhibitor Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Everolimus →

Package NDC codes (2)

Package NDCDescriptionSince
72319-017-0260 TABLET in 1 CONTAINER (72319-017-02)Aug 7, 2026
72319-017-6060 BLISTER PACK in 1 CARTON (72319-017-60) / 10 TABLET in 1 BLISTER PACK (72319-017-10)Aug 7, 2026

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