Suppliers / Joyang Laboratories

Joyang Laboratories

China Updated 9 July 2026

Joyang Laboratories is a finished-dose manufacturer based in China. It holds 9 active US drug master files and 3 valid CEPs across a filed portfolio of 9 molecules. Its GMP standing is certified by MFDS (Korea) and US FDA. Its most recent recorded inspection, by US FDA, closed on 25 April 2025 as VAI.

9
active US DMFs
3
valid CEPs
2
registered plants 1 with an FDA FEI number
2
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 25 April 2025 VAI US FDA
  • 22 August 2019 VAI US FDA
  • 5 May 2017 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Yancheng, China Not on file
China, China 3008639692

What they file, and where

Molecule Regulators Docs
Fusidic Acid EDQM, SFDA (Saudi Arabia), US FDA 4
Bacitracin US FDA 2
Adenosine US FDA 1
Cyclosporine US FDA 1
Mycophenolate Mofetil US FDA 1
Mycophenolic Acid US FDA 1
Pioglitazone US FDA 1
Sodium Fusidate EDQM 1
Tacrolimus EDQM 1

Also appears on these molecule pages

Adenosine finished dose Ciclosporin contract manufacturing Cyclosporine contract manufacturing Fusidic Acid finished dose Mycophenolate Mofetil finished dose Mycophenolic Acid finished dose Pioglitazone finished dose Tacrolimus contract manufacturing

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None
MFDS (Korea) None 2
US FDA None 1

Questions about Joyang Laboratories

Does Joyang Laboratories hold a US DMF or a CEP?
Joyang Laboratories holds 9 active US drug master files and 3 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.
Is Joyang Laboratories FDA-registered?
One site operated by Joyang Laboratories carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Joyang Laboratories's last inspection go?
The most recent inspection on record closed on 25 April 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does Joyang Laboratories manufacture?
2 registered sites are on record, in China (Yancheng and China). Every site is listed on this page with the register it came from.
What does Joyang Laboratories make?
9 molecules are on record against Joyang Laboratories, including Fusidic Acid, Bacitracin, Adenosine and Cyclosporine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Joyang Laboratories's GMP?
Current GMP certificates are on record from MFDS (Korea) and US FDA. 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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Open risk flags

  • The most recent inspection outcome was VAI, on 25 April 2025.

Comparable suppliers

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates