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Raunormin (DESERPIDINE)
Raunormin (Deserpidine) is a catecholamine-depleting sympatholytic small molecule originally developed by and currently owned by a pharmaceutical company. It targets the synaptic vesicular amine transporter, leading to a decrease in catecholamine levels in the synaptic cleft. Deserpidine was FDA-approved in 1957 for the treatment of hypertension and angina pectoris. Due to its off-patent status, there are currently no generic manufacturers. Key safety considerations include its potential to cause orthostatic hypotension and other cardiovascular side effects.
At a glance
| Generic name | DESERPIDINE |
|---|---|
| Drug class | Catecholamine-depleting Sympatholytic |
| Target | Synaptic vesicular amine transporter |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
| First approval | 1957 |
Approved indications
Common side effects
Primary sources
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| 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:
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