Suppliers / Shandong Haiyou Freda Pharmaceutical

Shandong Haiyou Freda Pharmaceutical

China Updated 9 July 2026

Shandong Haiyou Freda Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file and 2 valid CEPs across a filed portfolio of 3 molecules.

1
active US DMFs
2
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Linyi, China Not on file

What they file, and where

Molecule Regulators Docs
Gliclazide EDQM 1
Tadalafil EDQM 1
Upadacitinib US FDA 1

Also appears on these molecule pages

Gliclazide API Upadacitinib API Tadalafil API

Questions about Shandong Haiyou Freda Pharmaceutical

Does Shandong Haiyou Freda Pharmaceutical hold a US DMF or a CEP?
Shandong Haiyou Freda Pharmaceutical holds 1 active US drug master file and 2 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 Shandong Haiyou Freda Pharmaceutical manufacture?
1 registered site is on record, in China (Linyi). Every site is listed on this page with the register it came from.
What does Shandong Haiyou Freda Pharmaceutical make?
3 molecules are on record against Shandong Haiyou Freda Pharmaceutical, including Gliclazide, Tadalafil and Upadacitinib. 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