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Prescription medicine

Bremelanotide

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Bremelanotide used for?
The FDA-approved label (Vyleesi, Cosette Pharmaceuticals, Inc., November 13, 2025) says: “VYLEESI is indicated for the treatment of premenopausal women with acquired, generalized hypoactive sexual desire disorder (HSDD), as characterized by low sexual desire that causes marked distress or interpersonal difficulty and is NOT due to: A co-existing medical or psychiatric condition, Problems with the relationship, or The effects of a medication or drug substance. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Bremelanotide have a boxed warning?
No. None of the 1 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Bremelanotide?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Bremelanotide been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Bremelanotide?
1 company lists prescription products of Bremelanotide in the FDA NDC Directory, including Cosette Pharmaceuticals, Inc..

What Bremelanotide is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

VYLEESI is indicated for the treatment of premenopausal women with acquired, generalized hypoactive sexual desire disorder (HSDD), as characterized by low sexual desire that causes marked distress or interpersonal difficulty and is NOT due to: A co-existing medical or psychiatric condition, Problems with the relationship, or The effects of a medication or drug substance. …

— FDA label: Vyleesi, Cosette Pharmaceuticals, Inc., effective November 13, 2025. Read the full label on DailyMed →

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

Forms and how it is given

Dosage formsInjection
RouteSubcutaneous
Prescription products1 in the FDA NDC Directory
Brand namesVyleesi

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA210557
VYLEESI (AUTOINJECTOR)
CosetteJune 21, 2019 2, latest October 22, 2026
2026: Labeling · 2020: Labeling

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)2176316, 2176321
SPL set ID of the quoted labelf1d0c1b5-2f39-4bad-a6a4-0066e3ad5dcf
FDA labels (SPL)1
FDA applicationsNDA210557
Active ingredients (FDA)BREMELANOTIDE ACETATE

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Vyleesi, Cosette Pharmaceuticals, Inc., effective November 13, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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