femstat

Frequently asked questions

What does Femstat treat?

Femstat (Butoconazole Nitrate) may be used to treat vulvovaginal candidiasis, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.

How does Femstat work?

Femstat is a azole antifungal. Azole antifungals block a fungal enzyme (lanosterol 14-alpha-demethylase) that the fungus needs to make ergosterol, a key building block of its cell membrane. Without enough ergosterol the membrane becomes leaky and unstable, which stops the fungus from growing and can cause it to break apart and die.

Is there a coupon or discount for Femstat?

pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Femstat. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.

Who makes Femstat?

Femstat is marketed by Roche Palo. You can see Roche Palo's full profile, rating, and other products on pharmaranks.

Is Femstat a brand-name or generic drug?

Femstat is a brand-name product with the active ingredient Butoconazole Nitrate.

Is Femstat available over the counter?

No. Femstat is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.

What forms does Femstat come in?

Femstat is currently marketed as suppository and topical, per the FDA's National Drug Code Directory.

What class of drug is Femstat?

Femstat is classified as azole antifungal, per the FDA's Established Pharmacologic Class.

Is Femstat FDA-registered?

Femstat is on record with the U.S. FDA under application number NDA019359. You can verify this on its official FDA label.