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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 EGRIFTA WR in 香港. FDA-approved US medicine with a withdrawn EU application.

Current source route

EGRIFTA WR in 香港

Open exact country guide
Direct answer / 香港

Can you buy EGRIFTA WR in 香港?

FDA-approved US medicine with a withdrawn EU application

EGRIFTA WR is an FDA-approved US tesamorelin prescription product with an exact application, presentation, indication, label, and regulated supply chain. The European Egrifta marketing-authorisation application was withdrawn in 2012. Neither record authenticates research vials, compounded preparations, imported packages, or seller claims, and neither establishes current authorization or supply in another jurisdiction.

  1. 01
    Resolve the nameFDA-approved medicine
  2. 02
    Check 香港FDA-approved medicine
  3. 03
    Verify the exact offerProduct, seller, and supply route must match
Identity recordFDA-approved US medicine with a withdrawn EU application

What EGRIFTA WR resolves to

EGRIFTA WR is an FDA-approved US tesamorelin prescription product with an exact application, presentation, indication, label, and regulated supply chain. The European Egrifta marketing-authorisation application was withdrawn in 2012. Neither record authenticates research vials, compounded preparations, imported packages, or seller claims, and neither establishes current authorization or supply in another jurisdiction.

Evidence lane
FDA-approved medicine
Current record
BLA 022505 · FDA-approved prescription drug
Checked
July 17, 2026
tesamorelinEgrifta WREgrifta SVTH9507BLA 022505
Destination record註冊產品與持牌銷售商需分開核實

What 香港 still has to prove

本指南協助在香港搜尋肽類、肽類藥物、體重管理藥物或研究材料的人，利用衞生署藥物辦公室的註冊藥劑製品資料庫和持牌藥物銷售商搜尋，分別確認指定產品及法律銷售實體。網上名稱、港幣標價或本地送貨聲明都不是完整核實。核實時應記錄註冊編號、牌照類別、法定公司名稱、地址和查詢日期，讓每項供應聲明都能連回現行官方紀錄。

Comparison mode
HKD / 藥物辦公室產品及銷售商紀錄
Price coverage
尚無符合發布標準的香港銷售商價格表
Guide updated
2026年7月18日
Product record搜尋藥物資料庫香港衞生署藥物辦公室 ↗Seller or supply record搜尋持牌藥物銷售商香港衞生署藥物辦公室 ↗
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
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