Suppliers / Suzhou Tianlu Bio-pharmaceutical Co.,Ltd

Suzhou Tianlu Bio-pharmaceutical Co.,Ltd

China 2 employees Updated 9 July 2026

Suzhou Tianlu Bio-pharmaceutical Co.,Ltd is an API manufacturer based in China. It holds one valid CEP.

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

Registered plants

Site FDA FEI
Suzhou, China Not on file

What they file, and where

Molecule Regulators Docs
Ursodeoxycholic Acid EDQM 1

Also appears on these molecule pages

Ursodeoxycholic Acid API

Questions about Suzhou Tianlu Bio-pharmaceutical Co.,Ltd

Does Suzhou Tianlu Bio-pharmaceutical Co.,Ltd hold a US DMF or a CEP?
Suzhou Tianlu Bio-pharmaceutical Co.,Ltd holds 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 Suzhou Tianlu Bio-pharmaceutical Co.,Ltd manufacture?
1 registered site is on record, in China (Suzhou). Every site is listed on this page with the register it came from.
What does Suzhou Tianlu Bio-pharmaceutical Co.,Ltd make?
1 molecule is on record against Suzhou Tianlu Bio-pharmaceutical Co.,Ltd, including Ursodeoxycholic Acid. 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