United States · FDA National Drug Code directory
Dofetilide 0.125mg
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
- 70010-024_44f3f63d-4521-91e4-e063-6394a90a6d1b
- Product NDC
- 70010-024
- Form
- CAPSULE
- Composition / generic term
- Dofetilide 0.125mg
- Labeler
- Granules Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241114
- Source listing expiry
- 20261231
Source-listed ingredients
- DOFETILIDE — .125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE in 1 BOTTLE (70010-024-06) · 70010-024-06
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →