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
- 70301-2009_5a0e3578-8d3e-9e81-e063-6294a90a3795
- Product NDC
- 70301-2009
- Form
- CAPSULE
- Composition / generic term
- TEMOZOLOMIDE
- Labeler
- OPKO Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260822
- Source listing expiry
- 20271231
Source-listed ingredients
- TEMOZOLOMIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 PACKET in 1 CARTON (70301-2009-1) / 1 CAPSULE in 1 PACKET · 70301-2009-1
- 14 PACKET in 1 CARTON (70301-2009-2) / 1 CAPSULE in 1 PACKET · 70301-2009-2
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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