Methotrexate

NDC 62135-772 · Chartwell RX, LLC

Generic nameMethotrexate

Dosage formTABLET

RouteORAL

Active ingredient(s)METHOTREXATE SODIUM

Strength2.5 mg/1

Pharmacologic classFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

Marketing categoryANDA

Packages

62135-772-35 — 36 TABLET in 1 BOTTLE (62135-772-35)

FDA lists these products with the same active ingredient.

59137-525 — methotrexate, 59137-530 — methotrexate, 59137-535 — methotrexate, 59137-540 — methotrexate, 59137-550 — methotrexate, 59651-182 — Methotrexate, 61703-124 — Methotrexate, 61703-161 — Methotrexate, 61703-350 — Methotrexate, 61703-408 — Methotrexate, 62332-711 — methotrexate, 62332-712 — methotrexate, 62332-730 — METHOTREXATE, 63323-122 — METHOTREXATE SODIUM, 63323-123 — METHOTREXATE SODIUM, 64850-330 — Methotrexate Sodium, 67046-1524 — Methotrexate, 68071-3765 — Methotrexate, 68071-3991 — Methotrexate, 71335-0782 — Methotrexate, +34 more

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