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Nimotop (NIMODIPINE)

Azurity · FDA-approved approved Small molecule Quality 50/100

Nimotop (Nimodipine) is a dihydropyridine calcium channel blocker, a small molecule modality targeting the voltage-dependent L-type calcium channel subunit alpha-1F. It was originally developed and is currently owned by Azurity. FDA approved in 1988 for the treatment of subarachnoid intracranial hemorrhage, Nimotop is available as a generic medication with multiple manufacturers. Key safety considerations include its short half-life of 1.3 hours and low bioavailability of 11%. As an off-patent medication, Nimotop is widely available.

At a glance

Generic nameNIMODIPINE
SponsorAzurity
Drug classDihydropyridine Calcium Channel Blocker [EPC]
TargetVoltage-dependent L-type calcium channel subunit alpha-1F
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1988

Approved indications

Boxed warnings

Common side effects

Drug interactions

Key clinical trials

Patents

PatentExpiryType

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity