Suppliers / Aurisco Pharmaceutical Co.,Ltd

Aurisco Pharmaceutical Co.,Ltd

China 605116.SS 34 employees 2 duplicate records merged Updated 9 July 2026

Aurisco Pharmaceutical Co.,Ltd is an API manufacturer based in China. It holds 38 active US drug master files across a filed portfolio of 17 molecules. Its GMP standing is certified by MFDS (Korea).

38
active US DMFs
0
valid CEPs
0
registered plants
6
filings across 1 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 6 None
MFDS (Korea) None 2

Questions about Aurisco Pharmaceutical Co.,Ltd

Does Aurisco Pharmaceutical Co.,Ltd hold a US DMF or a CEP?
Aurisco Pharmaceutical Co.,Ltd holds 38 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 Aurisco Pharmaceutical Co.,Ltd make?
17 molecules are on record against Aurisco Pharmaceutical Co.,Ltd, including Flumethasone, Fluticasone Propionate, Abiraterone and Apalutamide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Aurisco Pharmaceutical Co.,Ltd's GMP?
Current GMP certificates are on record from MFDS (Korea). 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