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Mycophenolate Mofetil

NDC 31722-879 · Camber 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

31722-879-01 — 100 TABLET, FILM COATED in 1 BOTTLE (31722-879-01)

31722-879-05 — 500 TABLET, FILM COATED in 1 BOTTLE (31722-879-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0781-5175 — Mycophenolate Mofetil, 0904-7078 — Mycophenolate mofetil, 0904-7466 — mycophenolate mofetil, 16729-019 — mycophenolate mofetil, 16729-094 — mycophenolate mofetil, 23155-830 — Mycophenolate mofetil, 23155-836 — Mycophenolate mofetil, 23155-848 — MYCOPHENOLATE MOFETIL, 24338-018 — MYCOPHENOLATE MOFETIL, 31722-878 — Mycophenolate Mofetil, 42023-172 — mycophenolate mofetil, 50090-4275 — Mycophenolate Mofetil, 50268-557 — mycophenolate mofetil, 50268-558 — Mycophenolate Mofetil, 55154-3571 — Mycophenolate mofetil, 59651-624 — Mycophenolate mofetil, 59651-638 — Mycophenolate Mofetil, 59651-646 — mycophenolate mofetil, 60219-1595 — Mycophenolate Mofetil, 60687-438 — 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.