Suppliers / Zhejiang Ausun

Zhejiang Ausun

China reconciled across 11 public records · 2 entities Updated 9 July 2026

Zhejiang Ausun is an API manufacturer based in China. It holds 8 valid CEPs across a filed portfolio of 13 molecules. Its GMP standing is certified by EMA.

0
active US DMFs
8
valid CEPs
1
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Taizhou, China Not on file

What they file, and where

Molecule Regulators Docs
Ticagrelor EDQM, SFDA (Saudi Arabia) 4
Entecavir EDQM, SFDA (Saudi Arabia) 3
Apixaban SFDA (Saudi Arabia) 2
Febuxostat SFDA (Saudi Arabia) 2
Sugammadex SFDA (Saudi Arabia) 2
Entecavir Monohydrate EDQM 1
Imatinib Mesilate EDQM 1
Latanoprost EDQM 1
Macitentan SFDA (Saudi Arabia) 1
Nebivolol EDQM 1
Show all 13 molecules on file
Pilocarpine EDQM 1
Posaconazole SFDA (Saudi Arabia) 1
Tofacitinib SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1

Questions about Zhejiang Ausun

Does Zhejiang Ausun hold a US DMF or a CEP?
Zhejiang Ausun holds 8 valid CEPs. 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.
Where does Zhejiang Ausun manufacture?
1 registered site is on record, in China (Taizhou). Every site is listed on this page with the register it came from.
What does Zhejiang Ausun make?
13 molecules are on record against Zhejiang Ausun, including Ticagrelor, Entecavir, Apixaban and Febuxostat. Each links through to that molecule's full manufacturer list.
Which regulators recognise Zhejiang Ausun's GMP?
Current GMP certificates are on record from EMA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates