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.

Checking Suzhou Tianlu Bio-pharmaceutical Co.,Ltd?

Ask Fred what the record holds on Suzhou Tianlu Bio-pharmaceutical Co.,Ltd, including filings and inspection history.

Chat with Fred, your AI analyst
Opens WhatsApp. Free to start.

Comparable suppliers

Alivus Life Sciences shares 1 molecule Macleods Pharmaceuticals shares 1 molecule Solara Active Pharma Sciences shares 1 molecule Shilpa Pharma Lifesciences shares 1 molecule Dipharma Francis shares 1 molecule

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