United States · FDA National Drug Code directory
Dofetilide
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
- 42794-045_f1f1f93d-aee6-246f-e053-2a95a90a9eee
- Product NDC
- 42794-045
- Form
- CAPSULE
- Composition / generic term
- Dofetilide
- Labeler
- Sigmapharm Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180611
- Source listing expiry
- 20261231
Source-listed ingredients
- DOFETILIDE — 250 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE in 1 BOTTLE, PLASTIC (42794-045-10) · 42794-045-10
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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