Temozolomide

NDC 70301-2007 · OPKO Pharmaceuticals, LLC

Generic nameTEMOZOLOMIDE

Dosage formCAPSULE

RouteORAL

Active ingredient(s)TEMOZOLOMIDE

Strength140 mg/1

Pharmacologic classAlkylating Activity [MoA], Alkylating Drug [EPC]

Marketing categoryANDA

Packages

70301-2007-1 — 5 PACKET in 1 CARTON (70301-2007-1) / 1 CAPSULE in 1 PACKET

70301-2007-2 — 14 PACKET in 1 CARTON (70301-2007-2) / 1 CAPSULE in 1 PACKET

FDA lists these products with the same active ingredient.

65162-804 — Temozolomide, 65162-805 — Temozolomide, 65162-806 — Temozolomide, 67877-537 — Temozolomide, 67877-538 — Temozolomide, 67877-539 — Temozolomide, 67877-540 — Temozolomide, 67877-541 — Temozolomide, 67877-542 — Temozolomide, 70301-2005 — TEMOZOLOMIDE, 70301-2009 — TEMOZOLOMIDE, 70301-2011 — TEMOZOLOMIDE, 72162-2659 — Temozolomide, 72162-2660 — Temozolomide, 72162-2661 — Temozolomide, 72162-2662 — Temozolomide, 72162-2663 — Temozolomide, 72162-2664 — Temozolomide, 73043-011 — Temozolomide, 73043-012 — Temozolomide, +50 more

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