METHOTREXATE

NDC 55150-510 · Eugia US LLC

Generic nameMETHOTREXATE

Dosage formINJECTION, SOLUTION

RouteINTRAMUSCULAR, INTRATHECAL, INTRAVENOUS, SUBCUTANEOUS

Active ingredient(s)METHOTREXATE SODIUM

Strength50 mg/2mL

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

Marketing categoryANDA

Packages

55150-510-01 — 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-510-01) / 2 mL in 1 VIAL, SINGLE-DOSE

55150-510-05 — 5 VIAL, SINGLE-DOSE in 1 CARTON (55150-510-05) / 2 mL in 1 VIAL, SINGLE-DOSE

FDA lists these products with the same active ingredient.

46708-730 — METHOTREXATE, 47335-235 — Methotrexate Sodium, 48433-065 — methotrexate, 50090-5457 — Methotrexate, 51079-670 — methotrexate, 51285-366 — Methotrexate, 51285-367 — Methotrexate, 51285-368 — Methotrexate, 51285-369 — Methotrexate, 51407-121 — methotrexate, 55150-511 — METHOTREXATE, 55150-512 — METHOTREXATE, 55150-513 — METHOTREXATE, 59137-505 — methotrexate, 59137-510 — methotrexate, 59137-515 — methotrexate, 59137-520 — methotrexate, 59137-525 — methotrexate, 59137-530 — methotrexate, 59137-535 — 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.