CYCLOSPORINE

NDC 68180-214 · Lupin Pharmaceuticals, Inc.

Generic namecyclosporine

Dosage formEMULSION

RouteOPHTHALMIC

Active ingredient(s)CYCLOSPORINE

Strength.5 mg/mL

Pharmacologic classCalcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]

Marketing categoryNDA AUTHORIZED GENERIC

Packages

68180-214-30 — 30 VIAL, SINGLE-USE in 1 TRAY (68180-214-30) / .4 mL in 1 VIAL, SINGLE-USE

68180-214-60 — 60 VIAL, SINGLE-USE in 1 TRAY (68180-214-60) / .4 mL in 1 VIAL, SINGLE-USE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

23155-839 — CYCLOSPORINE, 24979-126 — cyclosporine, 47335-506 — cyclosporine, 47335-507 — cyclosporine, 50090-4476 — cyclosporine, 60505-0133 — Cyclosporine, 60505-0134 — Cyclosporine, 60505-4630 — Cyclosporine, 60505-4631 — Cyclosporine, 60505-4632 — Cyclosporine, 60505-6202 — Cyclosporine, 65086-001 — cyclosporine, 68084-879 — Cyclosporine, 68084-921 — Cyclosporine, 71656-012 — CYCLOSPORINE, 73043-005 — cyclosporine, 75907-047 — Cyclosporine, 75907-048 — Cyclosporine, 82667-014 — cyclosporine, 82667-900 — cyclosporine ophthalmic solution, +19 more

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