NDC 0093-7769 – Everolimus

Everolimus 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-7769

Product details

Brand name
Everolimus
Generic name
Everolimus
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210050
Marketed since
October 23, 2023
Marketing end
September 30, 2026
Pharmacologic class
Kinase Inhibitor; mTOR Inhibitor Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Everolimus →

Package NDC codes (1)

Package NDCDescriptionSince
0093-7769-2428 BLISTER PACK in 1 CARTON (0093-7769-24) / 1 TABLET in 1 BLISTER PACK (0093-7769-19)Oct 23, 2023

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