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Peptide Atlas

Peptide Regulatory Status

Understanding regulations across different countries

FDA Approved Peptides

Tirzepatide

FDA Regulatory Status

FDA Approved

Approved: May 13, 2022

Approved Indication:

Type 2 diabetes mellitus, chronic weight management

Clinical Trial Phase:

Phase 4 (Post-Marketing)

Approved as Mounjaro for diabetes. Approved as Zepbound for chronic weight management.

Source: FDA.gov
Last updated: Jan 15, 2024

Regulatory History

November 8, 2023

FDA approval for chronic weight management (Zepbound)

Source: FDA.gov

May 13, 2022

FDA approval for Type 2 diabetes (Mounjaro)

Source: FDA.gov

FDA regulatory information is provided for informational purposes only and may not be current or complete. Regulations can change frequently. Always consult with FDA.gov and qualified regulatory experts for the most current information.

Peptides in Clinical Trials

Tirzepatide

Phase 4 (Post-Marketing)

Important Regulatory Disclaimer

Regulatory information provided on this site is for informational purposes only and may not be current, complete, or accurate. Peptide regulations vary by country and can change frequently. Always consult with local regulatory authorities, legal counsel, and healthcare professionals before purchasing, importing, or using peptides in your country. The information provided does not constitute legal or medical advice.

Understanding Regulatory Status

Approved

Peptide is approved for medical use in this country, typically requiring a prescription.

Research Only

Peptide is permitted for research purposes only, not for human consumption or therapeutic use.

Prescription Required

Peptide requires a valid prescription from a licensed healthcare provider.

Restricted

Peptide is restricted or controlled, with specific conditions for use or import.

Prohibited

Peptide is prohibited for import, sale, or use in this country.

Country-Specific Information

Regulatory status for each peptide is displayed on individual peptide pages. Select a country to view the current regulatory status and any relevant notes or restrictions.

For the most up-to-date information, always consult:

  • Local regulatory authorities (FDA, Health Canada, MHRA, etc.)
  • Customs and import regulations
  • Licensed healthcare providers
  • Legal counsel familiar with pharmaceutical regulations