Identity recordProduct-specific FDA-approved US medicine record
What VYLEESI resolves to
VYLEESI is the FDA-approved US bremelanotide 1.75 mg autoinjector with an exact application, indication, label, presentation, and regulated prescription supply chain. That approval does not transfer to seller-labelled PT-141 research vials, compounded products, imported presentations, online listings, or supply routes, and it does not establish authorization or current availability in another country.
- Evidence lane
- FDA-approved medicine
- Current record
- NDA 210557 · FDA-approved prescription drug
- Checked
- July 17, 2026
bremelanotideVyleesiPT-141NDA 210557melanocortin receptor agonist
Destination recordPemeriksaan produk BPOM dan distribusi wajib
What Indonesia still has to prove
Panduan Indonesia untuk mencocokkan klaim produk terkait peptida di Cek BPOM dan memeriksa bukti distribusi farmasi yang tersertifikasi, masih berlaku, atau telah dicabut melalui catatan CDOB publik sebelum menilai penjual, produk impor, pasar daring, bahan riset, atau jalur pasok.
- Comparison mode
- Rupiah / catatan produk BPOM dan distribusi CDOB
- Price coverage
- Belum ada tabel penjual Indonesia yang memenuhi syarat
- Guide updated
- 18 Juli 2026