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FULVICIN P/G 330 (GRISEOFULVIN, ULTRAMICROSIZE)

CHARTWELL RX · FDA-approved approved ✓ Verified May 2026 Quality 23/100

FULVICIN P/G 330 (generic name: GRISEOFULVIN, ULTRAMICROSIZE) is a drug developed by CHARTWELL RX. It is currently FDA-approved for Onychomycosis due to dermatophyte, Tinea barbae, Tinea capitis.

FULVICIN P/G 330 is a small molecule inhibitor that targets tubulin. It is classified as a tubulin inhibitor, which is a type of drug that works by interfering with the function of tubulin, a protein involved in cell division.

At a glance

Generic nameGRISEOFULVIN, ULTRAMICROSIZE
SponsorCHARTWELL RX
TargetLanosterol 14-alpha demethylase, Solute carrier family 22 member 1, Tubulin
Therapeutic areaDermatology
PhaseFDA-approved

Approved indications

Common side effects

Serious adverse events

Competitive intelligence

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Frequently asked questions about FULVICIN P/G 330

What is FULVICIN P/G 330?

FULVICIN P/G 330 (GRISEOFULVIN, ULTRAMICROSIZE) is a pharmaceutical drug developed by CHARTWELL RX, indicated for Onychomycosis due to dermatophyte, Tinea barbae, Tinea capitis.

What is FULVICIN P/G 330 used for?

FULVICIN P/G 330 is indicated for Onychomycosis due to dermatophyte, Tinea barbae, Tinea capitis, Tinea corporis, Tinea cruris.

Who makes FULVICIN P/G 330?

FULVICIN P/G 330 is developed and marketed by CHARTWELL RX (see full CHARTWELL RX pipeline at /company/chartwell-rx).

What is the generic name of FULVICIN P/G 330?

GRISEOFULVIN, ULTRAMICROSIZE is the generic (nonproprietary) name of FULVICIN P/G 330.

What development phase is FULVICIN P/G 330 in?

FULVICIN P/G 330 is FDA-approved (marketed).

What are the side effects of FULVICIN P/G 330?

Common side effects of FULVICIN P/G 330 include Skin rashes, Urticaria, Nausea, Vomiting, Epigastric distress, Diarrhea. Serious adverse events: Erythema multiforme-like drug reactions, Angioneurotic edema, Severe skin adverse events, Severe hepatic adverse events.

What does FULVICIN P/G 330 target?

FULVICIN P/G 330 targets Lanosterol 14-alpha demethylase, Solute carrier family 22 member 1, Tubulin.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing