United States · FDA National Drug Code directory
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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
- 58468-7820_abb9eb38-c6a9-49e9-8e90-852f95773feb
- Product NDC
- 58468-7820
- Form
- TABLET, FILM COATED
- Composition / generic term
- Vandetanib
- Labeler
- Genzyme Corporation
- Marketing category
- NDA
- Marketing start / end (source format)
- 20110725
- Source listing expiry
- 20271231
Source-listed ingredients
- VANDETANIB — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (58468-7820-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 58468-7820-3
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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