Last reviewed · How we verify

Grifulvin V (GRISEOFULVIN)

Johnson And Johnson · FDA-approved approved Small molecule Quality 51/100

Grifulvin V (GRISEOFULVIN) is a small molecule tubulin inhibiting agent developed by WYETH AYERST and currently owned by Johnson and Johnson. It targets the solute carrier family 22 member 1 and was FDA approved in 1962 for the treatment of various fungal infections, including onychomycosis, tinea barbae, tinea capitis, tinea corporis, tinea cruris, and tinea pedis. Grifulvin V is available as a generic medication due to its off-patent status. Key safety considerations include potential gastrointestinal side effects and interactions with other medications. It has a bioavailability of 48%.

At a glance

Generic nameGRISEOFULVIN
SponsorJohnson And Johnson
Drug classTubulin Inhibiting Agent [EPC]
TargetSolute carrier family 22 member 1
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved
First approval1962

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: