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EVEROLIMUS

NDC 70377-012 · Biocon Pharma Inc.

Generic nameeverolimus
Dosage formTABLET
RouteORAL
Active ingredient(s)EVEROLIMUS
Strength7.5 mg/1
Pharmacologic classCytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]
Marketing categoryANDA

Packages

70377-012-11 — 30 TABLET in 1 BOTTLE (70377-012-11)

70377-012-22 — 4 BLISTER PACK in 1 CARTON (70377-012-22) / 7 TABLET in 1 BLISTER PACK

70377-012-23 — 4 BLISTER PACK in 1 CARTON (70377-012-23) / 7 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63850-0062 — Everolimus, 63850-0063 — Everolimus, 63850-0064 — Everolimus, 63850-0107 — Everolimus, 67877-718 — Everolimus, 67877-719 — Everolimus, 67877-720 — Everolimus, 67877-721 — Everolimus, 70377-010 — everolimus, 70377-011 — everolimus, 70377-013 — everolimus, 70377-069 — Everolimus, 70377-070 — EVEROLIMUS, 70377-071 — everolimus, 70377-090 — Everolimus, 70377-091 — Everolimus, 70377-092 — Everolimus, 70377-112 — everolimus, 72603-254 — everolimus, 72603-255 — everolimus, +63 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.