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
- 47335-890_7c774570-443b-40da-8038-7cb550f92048
- Product NDC
- 47335-890
- Form
- CAPSULE
- Composition / generic term
- Temozolomide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140213
- Source listing expiry
- 20261231
Source-listed ingredients
- TEMOZOLOMIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (47335-890-21) / 14 CAPSULE in 1 BOTTLE · 47335-890-21
- 15 BLISTER PACK in 1 CARTON (47335-890-72) / 1 CAPSULE in 1 BLISTER PACK · 47335-890-72
- 5 BLISTER PACK in 1 CARTON (47335-890-74) / 1 CAPSULE in 1 BLISTER PACK · 47335-890-74
- 20 BLISTER PACK in 1 CARTON (47335-890-75) / 1 CAPSULE in 1 BLISTER PACK · 47335-890-75
- 1 BOTTLE in 1 CARTON (47335-890-80) / 5 CAPSULE in 1 BOTTLE · 47335-890-80
- 1 BOTTLE in 1 CARTON (47335-890-87) / 20 CAPSULE in 1 BOTTLE · 47335-890-87
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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