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Mycophenolate mofetil

NDC 68071-3767 · NuCare Pharmaceuticals, Inc.

Generic nameMycophenolate mofetil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)MYCOPHENOLATE MOFETIL
Strength500 mg/1
Pharmacologic classAntimetabolite Immunosuppressant [EPC]
Marketing categoryANDA

Packages

68071-3767-6 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-885 — mycophenolate mofetil, 63629-9582 — mycophenolate mofetil, 64380-725 — Mycophenolate mofetil, 64380-726 — Mycophenolate mofetil, 65050-2073 — Mycophenolate Mofetil, 66689-307 — Mycophenolate Mofetil, 67457-386 — Mycophenolate Mofetil, 67877-225 — Mycophenolate Mofetil, 67877-230 — Mycophenolate mofetil, 67877-266 — mycophenolate mofetil, 68254-5000 — mycophenolate mofetil, 68254-5003 — MYCOPHENOLATE MOFETIL, 69238-1595 — Mycophenolate Mofetil, 70518-2767 — Mycophenolate mofetil, 70518-3799 — Mycophenolate mofetil, 70518-4036 — MYCOPHENOLATE MOFETIL, 70518-4377 — Mycophenolate mofetil, 70752-294 — Mycophenolate Mofetil, 71288-803 — Mycophenolate Mofetil, 71610-033 — mycophenolate mofetil, +36 more

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