Cyclophosphamide

NDC 68001-695 · BluePoint Laboratories

Generic namecyclophosphamide

Dosage formINJECTION, POWDER, FOR SOLUTION

RouteINTRAVENOUS, ORAL

Active ingredient(s)CYCLOPHOSPHAMIDE

Strength1 g/50mL

Marketing categoryANDA

Packages

68001-695-32 — 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-695-32) / 50 mL in 1 VIAL, SINGLE-DOSE

FDA lists these products with the same active ingredient.

55150-272 — Cyclophosphamide, 62332-618 — Cyclophosphamide, 62332-619 — Cyclophosphamide, 65219-131 — cyclophosphamide, 65219-133 — cyclophosphamide, 65219-135 — cyclophosphamide, 68001-442 — cyclophosphamide, 68001-443 — cyclophosphamide, 68001-444 — cyclophosphamide, 68001-694 — cyclophosphamide, 68001-696 — cyclophosphamide, 68275-222 — Cyclophosphamide, 69097-516 — Cyclophosphamide, 69097-517 — Cyclophosphamide, 70121-1238 — Cyclophosphamide, 70121-1239 — Cyclophosphamide, 70121-1240 — Cyclophosphamide, 70301-2013 — CYCLOPHOSPHAMIDE, 70301-2015 — CYCLOPHOSPHAMIDE, 70436-105 — Cyclophosphamide for Injection, +62 more

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