United States · FDA National Drug Code directory

Temozolomide

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
73043-012_d6ae8576-1b18-45d5-b651-cc290d979032
Product NDC
73043-012
Form
CAPSULE
Composition / generic term
Temozolomide
Labeler
Devatis, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170428
Source listing expiry
20261231

Source-listed ingredients

  • TEMOZOLOMIDE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 CAPSULE in 1 BOTTLE (73043-012-05) · 73043-012-05
  • 14 CAPSULE in 1 BOTTLE (73043-012-14) · 73043-012-14

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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