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PEMRYDI RTU

NDC 70121-2462 · Amneal Pharmaceuticals LLC

Generic namePemetrexed disodium
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)PEMETREXED DISODIUM HEMIPENTAHYDRATE
Strength1000 mg/100mL
Pharmacologic classFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
Marketing categoryNDA

Packages

70121-2462-1 — 1 VIAL in 1 CARTON (70121-2462-1) / 100 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-337 — Pemetrexed disodium, 43547-632 — Pemetrexed, 55150-381 — Pemetrexed, 55150-382 — Pemetrexed, 55150-383 — Pemetrexed, 63759-3048 — Pemetrexed disodium, 63759-3049 — Pemetrexed disodium, 63759-3050 — Pemetrexed disodium, 67184-0503 — Pemetrexed disodium, 67184-0504 — Pemetrexed disodium, 68001-535 — Pemetrexed, 68001-536 — Pemetrexed, 68001-538 — Pemetrexed disodium, 68001-539 — Pemetrexed disodium, 70121-2453 — Pemetrexed disodium, 70121-2461 — Pemetrexed disodium, 71288-166 — Pemetrexed disodium, 71288-167 — Pemetrexed disodium, 72603-325 — Pemetrexed disodium, 72603-425 — Pemetrexed disodium, +6 more

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