Suppliers / Chengdu Yacht Biotechnology

Chengdu Yacht Biotechnology

China 2 employees Updated 9 July 2026

Chengdu Yacht Biotechnology is an API manufacturer based in China. It holds 11 active US drug master files across a filed portfolio of 9 molecules.

11
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Daptomycin US FDA 2
Everolimus US FDA 2
Anidulafungin US FDA 1
Caspofungin US FDA 1
Dalbavancin US FDA 1
Mupirocin US FDA 1
Pimecrolimus US FDA 1
Polymyxin B US FDA 1
Tacrolimus US FDA 1

Also appears on these molecule pages

Questions about Chengdu Yacht Biotechnology

Does Chengdu Yacht Biotechnology hold a US DMF or a CEP?
Chengdu Yacht Biotechnology holds 11 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
What does Chengdu Yacht Biotechnology make?
9 molecules are on record against Chengdu Yacht Biotechnology, including Daptomycin, Everolimus, Anidulafungin and Caspofungin. Each links through to that molecule's full manufacturer list.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability