METHOTREXATE

NDC 46708-730 · Alembic Pharmaceuticals Limited

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

46708-730-31 — 100 TABLET in 1 BOTTLE (46708-730-31)

46708-730-36 — 36 TABLET in 1 BOTTLE (46708-730-36)

FDA lists these products with the same active ingredient.

0054-4550 — Methotrexate Sodium, 0378-0014 — methotrexate, 0555-0572 — Methotrexate, 0703-3671 — Methotrexate, 0703-3675 — Methotrexate, 0703-3678 — Methotrexate, 16729-486 — Methotrexate, 42291-594 — Methotrexate, 46708-711 — methotrexate, 46708-712 — 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, 55150-510 — 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.