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Methotrexate

NDC 71335-0782 · Bryant Ranch Prepack

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

71335-0782-1 30 TABLET in 1 BOTTLE (71335-0782-1)

71335-0782-2 12 TABLET in 1 BOTTLE (71335-0782-2)

71335-0782-3 20 TABLET in 1 BOTTLE (71335-0782-3)

71335-0782-4 100 TABLET in 1 BOTTLE (71335-0782-4)

71335-0782-5 36 TABLET in 1 BOTTLE (71335-0782-5)

71335-0782-6 24 TABLET in 1 BOTTLE (71335-0782-6)

71335-0782-7 90 TABLET in 1 BOTTLE (71335-0782-7)

71335-0782-8 4 TABLET in 1 BOTTLE (71335-0782-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

61703-124 — Methotrexate, 61703-161 — Methotrexate, 61703-350 — Methotrexate, 61703-408 — Methotrexate, 62135-772 — 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, 71335-1118 — methotrexate, 71335-1772 — Methotrexate, 71335-2221 — Methotrexate, 72162-2174 — Methotrexate Sodium, 72162-2647 — METHOTREXATE, 82804-136 — Methotrexate, +34 more

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