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Vasodil (TOLAZOLINE)
Vasodil (TOLAZOLINE) is a small molecule drug developed by NOVARTIS that targets the Alpha-2A adrenergic receptor. It is classified as a tolazoline and was first approved by the FDA in 1948 for the treatment of cerebrovascular disease, disorders of blood vessels, and persistent pulmonary hypertension of the newborn. As an off-patent medication with no active Orange Book patents, Vasodil is available without generic competition. Key safety considerations include the need for careful dosing and monitoring due to its potent vasodilatory effects. NOVARTIS remains the current owner of the medication.
At a glance
| Generic name | TOLAZOLINE |
|---|---|
| Sponsor | Novartis |
| Drug class | tolazoline |
| Target | Alpha-2A adrenergic receptor |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
| First approval | 1948 |
Approved indications
- Cerebrovascular disease
- Disorder of blood vessel
- Persistent pulmonary hypertension of the newborn
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:
- Vasodil CI brief — competitive landscape report
- Vasodil updates RSS · CI watch RSS
- Novartis portfolio CI