This is preserved historical wording.
It is no longer the current profile. Read the current profile and its correction notice.
It is no longer the current profile. Read the current profile and its correction notice.
What this version reported
FDA's substance registry identifies TB-500 as an N-terminal acetylated 17-23 fragment of thymosin beta-4 and explicitly states that a UNII record does not imply regulatory review or approval.↗
Organizations named in cited records:
- U.S. Food and Drug Administration↗
Sources for this version
- 1TB-500 substance identity record ↗
FDA Global Substance Registration System · Official source · Source checked July 29, 2026