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Acylanid (ACETYLDIGITOXIN)
Acetyldigitoxin, also known as Acylanid, is a small molecule drug developed by Novartis that targets the sodium/potassium-transporting ATPase. It is used to treat atrial fibrillation and congestive heart failure. The drug is off-patent, meaning it is no longer protected by patents, and there are no generic manufacturers. Acetyldigitoxin was approved by the FDA in 1975 and has a bioavailability of 70%. As an off-patent drug, its commercial status is uncertain.
At a glance
| Generic name | ACETYLDIGITOXIN |
|---|---|
| Sponsor | Novartis |
| Drug class | acetyldigitoxin |
| Target | Sodium/potassium-transporting ATPase |
| Modality | Small molecule |
| Therapeutic area | Metabolic |
| Phase | FDA-approved |
| First approval | 1975 |
Approved indications
- Atrial fibrillation
- Congestive heart failure
Common side effects
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Acylanid CI brief — competitive landscape report
- Acylanid updates RSS · CI watch RSS
- Novartis portfolio CI