Cyclophosphamide

NDC 10019-982 · Baxter Healthcare Corporation

Generic nameCyclophosphamide

Dosage formTABLET

RouteORAL

Active ingredient(s)CYCLOPHOSPHAMIDE

Strength25 mg/1

Marketing categoryNDA AUTHORIZED GENERIC

Packages

10019-982-01 — 1 BOTTLE in 1 CARTON (10019-982-01) / 100 TABLET in 1 BOTTLE (10019-982-09)

FDA lists these products with the same active ingredient.

10019-937 — cyclophosphamide, 10019-938 — cyclophosphamide, 10019-939 — cyclophosphamide, 10019-942 — cyclophosphamide, 10019-943 — cyclophosphamide, 10019-944 — cyclophosphamide, 10019-945 — cyclophosphamide, 10019-955 — cyclophosphamide, 10019-956 — cyclophosphamide, 10019-957 — cyclophosphamide, 10019-984 — Cyclophosphamide, 14335-470 — Cyclophosphamide for Injection, 14335-471 — Cyclophosphamide for Injection, 14335-472 — Cyclophosphamide for Injection, 14789-125 — Cyclophosphamide, 14789-126 — Cyclophosphamide, 16714-857 — cyclophosphamide, 16714-858 — cyclophosphamide, 16714-859 — cyclophosphamide, 25021-247 — Cyclophosphamide, +62 more

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