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One name + one destination

Peptide status
by country.

Check whether a name resolves to a research listing, investigational program, or approved medicine, then open the exact product and seller records for the destination country.

Identity+Destination=Verification route
41tracked names
42country guides
3separate evidence lanes
99official source routes
Global source router

Two selections. No category shortcuts.

Start with a peptide name and destination. The result shows what the name means in our evidence database and which local records must be checked next.

Status check updated to VYLEESI in 日本. Product-specific FDA-approved US medicine record.

Current source route

VYLEESI in 日本

Open exact country guide
Direct answer / 日本

Can you buy VYLEESI in 日本?

Product-specific FDA-approved US medicine record

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.

  1. 01
    Resolve the nameFDA-approved medicine
  2. 02
    Check 日本FDA-approved medicine
  3. 03
    Verify the exact offerProduct, seller, and supply route must match
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 recordPMDAの製品単位の確認が必要

What 日本 still has to prove

日本でペプチド、ペプチド医薬品、減量薬、研究用材料を検索する人のために、PMDAの承認品目情報、電子添文、審査報告書、安全性情報を確認する手順をまとめたガイドです。一般名が一致するだけで承認製品、販売主体、供給経路まで同一と判断せず、英訳資料と最新の日本語記録の役割も分けて扱います。

Comparison mode
日本円 / PMDA承認、電子添文、安全性記録
Price coverage
公開基準を満たす国内販売者表は未掲載
Guide updated
2026年7月18日
Product record承認品目情報独立行政法人医薬品医療機器総合機構（PMDA） ↗Seller or supply record製品、安全性、電子添文、審査情報の検索入口独立行政法人医薬品医療機器総合機構（PMDA） ↗
Evidence coverageRouting records only

No compound-specific official record is attached to this exact pairing yet. That is an evidence gap, not proof of approval, prohibition, availability, or absence. Use the country guide and official product and seller routes to verify the exact offer.

Open the full country check
Result boundaryIdentity match ≠ destination approval ≠ verified seller

This check routes each question to the right record. It is not a medical recommendation, legal opinion, local availability claim, or commercial ranking.

Popular starting points

Open a common peptide and country check.

Each selection has a shareable URL, so you can send someone the exact peptide and destination without losing the identity or country context.

01CagriSema in South AfricaInvestigational clinical program02CagriSema in PortugalInvestigational clinical program03Retatrutide in ArgentinaInvestigational clinical program04Melanotan II in ItaliaUS research-market identity05PT-141 / Bremelanotide in ItaliaUS research-market identity with a separate FDA-approved medicine record06CJC-1295 DAC in FranceUS research-market identity07BPC-157 in FranceUS research-market identity08BPC-157 in DeutschlandUS research-market identity09Retatrutide in MéxicoInvestigational clinical program10Mazdutide in 中国China-approved medicine and active clinical program11Ecnoglutide in 中国China-approved medicine and active development program12Enicepatide in FranceInvestigational clinical program13Eloralintide in DeutschlandInvestigational clinical program14Tirzepatide in CanadaUS FDA medicine reference15Cagrilintide in United KingdomInvestigational clinical program16Petrelintide in DeutschlandInvestigational clinical program17MariTide in AustraliaInvestigational clinical program18Survodutide in FranceInvestigational clinical program19VK2735 in United StatesInvestigational clinical program20Pemvidutide in United StatesInvestigational clinical program21Semaglutide in الإمارات العربية المتحدةProduct-specific approved medicine records in multiple jurisdictions22Semaglutide in FranceProduct-specific approved medicine records in multiple jurisdictions23Semaglutide in CanadaProduct-specific approved medicine records in multiple jurisdictions24TB-500 in United StatesUS research-market identity25TB-500 in CanadaUS research-market identity26GHK-Cu in CanadaUS research-market identity27Semax in South AfricaUS research-market identity28Melanotan II in AustraliaUS research-market identity29MOTS-c in CanadaUS research-market identity30Tesamorelin in United StatesUS research-market identity with a separate FDA-licensed medicine record31AOD-9604 in South AfricaUS research-market identity with a failed oral obesity program and no FDA-approved drug32Ipamorelin in CanadaUS research-market identity33Selank in South AfricaUS research-market identity34PT-141 / Bremelanotide in United StatesUS research-market identity with a separate FDA-approved medicine record35CJC-1295 no DAC in CanadaUS research-market identity36CJC-1295 DAC in South AfricaUS research-market identity
Direct answers

What a country check means.

The short answer is a routing decision, not a blanket legal, medical, or availability conclusion.

01

Is BPC-157 legal in every European country?

No region-wide answer is supportable from a seller page or a single database. Resolve the BPC-157 identity, choose the exact destination, then check that country’s product and seller or supply records.

02

Is retatrutide available as an approved medicine?

The Peptide Local identity record places retatrutide in the investigational clinical-program lane. A seller-labelled vial cannot inherit the sponsor’s trial material, evidence, or regulatory status.

03

Does a tirzepatide record prove local availability?

No. The FDA reference resolves the US medicine identity. Authorization, presentation, prescription status, current market presence, and seller authority must still be confirmed in the selected country.

Why the split matters

A matching name is only the first record.

  1. 01

    Resolve identity

    Keep the active ingredient, research label, clinical program, sponsor code, and approved brand attached to their proper source.

  2. 02

    Resolve destination

    Open the national product database and the separate pharmacy, establishment, professional, seller, or supply record linked for that country.

  3. 03

    Resolve the exact offer

    Match the legal seller identity, product presentation, claimed category, current status, and delivery route. Do not transfer evidence between unlike products.

Continue the evidence trail
Search the complete peptide database ↗Compare all five world regions ↗Open all country, province, state, region, and city guides ↗