Temozolomide

NDC 47335-930 · Sun Pharmaceutical Industries, Inc.

Generic nameTemozolomide

Dosage formCAPSULE

RouteORAL

Active ingredient(s)TEMOZOLOMIDE

Strength180 mg/1

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

Marketing categoryANDA

Packages

47335-930-21 — 1 BOTTLE in 1 CARTON (47335-930-21) / 14 CAPSULE in 1 BOTTLE

47335-930-72 — 15 BLISTER PACK in 1 CARTON (47335-930-72) / 1 CAPSULE in 1 BLISTER PACK

47335-930-74 — 5 BLISTER PACK in 1 CARTON (47335-930-74) / 1 CAPSULE in 1 BLISTER PACK

47335-930-75 — 20 BLISTER PACK in 1 CARTON (47335-930-75) / 1 CAPSULE in 1 BLISTER PACK

47335-930-80 — 1 BOTTLE in 1 CARTON (47335-930-80) / 5 CAPSULE in 1 BOTTLE

47335-930-87 — 1 BOTTLE in 1 CARTON (47335-930-87) / 20 CAPSULE in 1 BOTTLE

J8700 — Temozolomide, oral, 5 mg Medicare Part B payment limit (ASP + 6%): $0.42

FDA lists these products with the same active ingredient.

31722-412 — TEMOZOLOMIDE, 31722-413 — TEMOZOLOMIDE, 31722-414 — TEMOZOLOMIDE, 31722-415 — TEMOZOLOMIDE, 31722-416 — TEMOZOLOMIDE, 47335-890 — Temozolomide, 47335-891 — Temozolomide, 47335-892 — Temozolomide, 47335-893 — Temozolomide, 47335-929 — Temozolomide, 65162-801 — Temozolomide, 65162-802 — Temozolomide, 65162-803 — Temozolomide, 65162-804 — Temozolomide, 65162-805 — Temozolomide, 65162-806 — Temozolomide, 67877-537 — Temozolomide, 67877-538 — Temozolomide, 67877-539 — Temozolomide, 67877-540 — 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.