Bortezomib

NDC 31722-303 · Camber Pharmaceuticals, Inc.

Generic nameBortezomib

Dosage formINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

RouteINTRAVENOUS, SUBCUTANEOUS

Active ingredient(s)BORTEZOMIB

Strength3.5 mg/1

Pharmacologic classProteasome Inhibitor [EPC], Proteasome Inhibitors [MoA]

Marketing categoryANDA

Packages

31722-303-31 — 1 VIAL, SINGLE-DOSE in 1 CARTON (31722-303-31) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

FDA lists these products with the same active ingredient.

0143-9098 — bortezomib, 0409-1700 — Bortezomib, 0409-1703 — BORTEZOMIB, 0409-1704 — BORTEZOMIB, 25021-262 — BORTEZOMIB, 43598-426 — Bortezomib, 51817-586 — bortezomib, 55150-337 — BORTEZOMIB, 60505-6050 — bortezomib, 63020-049 — bortezomib, 63323-821 — Bortezomib, 63759-3032 — Bortezomib, 67184-0530 — Bortezomib, 68001-534 — Bortezomib, 68001-540 — Bortezomib, 68001-541 — Bortezomib, 68083-650 — Bortezomib, 68083-651 — Bortezomib, 70069-836 — bortezomib, 70121-2484 — Bortezomib, +11 more

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