Suppliers / Shandong Yuwang Pharmaceutical

Shandong Yuwang Pharmaceutical

China 9 employees Updated 9 July 2026

Shandong Yuwang Pharmaceutical is an API manufacturer based in China. It holds 2 active US drug master files and one valid CEP across a filed portfolio of 3 molecules. Its filings concentrate with INVIMA (CO) and JFDA (JO).

2
active US DMFs
1
valid CEPs
1
registered plants
4
filings across 2 regulators

Registered plants

Site FDA FEI
Yucheng City, China Not on file

What they file, and where

Molecule Regulators Docs
Fish Oil US FDA 1
Omega-3-Acid Ethyl Esters US FDA 1
Omega-3-Acid Ethyl Esters 90 EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 3 None
JFDA (JO) 1 None

Questions about Shandong Yuwang Pharmaceutical

Does Shandong Yuwang Pharmaceutical hold a US DMF or a CEP?
Shandong Yuwang Pharmaceutical holds 2 active US drug master files and 1 valid CEP. 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 Shandong Yuwang Pharmaceutical manufacture?
1 registered site is on record, in China (Yucheng City). Every site is listed on this page with the register it came from.
What does Shandong Yuwang Pharmaceutical make?
3 molecules are on record against Shandong Yuwang Pharmaceutical, including Fish Oil, Omega-3-Acid Ethyl Esters and Omega-3-Acid Ethyl Esters 90. Each links through to that molecule's full manufacturer list.
Where does Shandong Yuwang Pharmaceutical file?
Filings are on record with INVIMA (CO) and JFDA (JO), 4 in total.

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