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Xiushi Biopharma

China (Nantong) • Manufacturer

Xiushi Biopharma is a peptide manufacturer based in China (Nantong). Direct manufacturer. Holds US DMFs for semaglutide, tirzepatide, retatrutide API.

ConfidenceMedium
Business TypeManufacturer
ModelManufacturer
RegionAsia
Verification status based on publicly available information and supplier-provided materials.

Listing reviewed October 2026.

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Nantong-based company producing peptide APIs by large-scale biosynthesis rather than chemical synthesis, with semaglutide and copper tripeptide-1 as its main products. Holds active US Drug Master Files for retatrutide, semaglutide and tirzepatide API across its Nantong and Rudong entities. No FDA inspection is on record.

Directory assessment: Xiushi Biopharma is listed as a manufacturer in the peptide supply chain, serving Asia markets from China (Nantong). As a direct manufacturer, this supplier controls its own production process from synthesis through purification and quality control release testing. This profile lists 2 sources for reference. This supplier has a medium confidence score — verification signals are present, but the listing is newer or less documented; perform standard due diligence before engaging.

Products (2)
peptide APIscosmetic peptides
Capabilities
US Drug Master Files
  • Retatrutide: DMF 44902 (Type II, active), submitted 2026-09-25
  • Semaglutide: DMFs 41460, 44827 (Type II, active), first submitted 2025-03-12
  • Tirzepatide: DMF 43983 (Type II, active), submitted 2026-03-30

DMF numbers from the FDA quarterly DMF list. A filed DMF is not FDA approval; its contents are confidential. Reviewed 2026-10-23.