Suppliers / Shenzhen Salubris Pharmaceuticals

Shenzhen Salubris Pharmaceuticals

China 30 employees Updated 9 July 2026

Shenzhen Salubris Pharmaceuticals is an API manufacturer based in China. It holds 2 active US drug master files and 2 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by ANVISA (Brazil).

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

Registered plants

Site FDA FEI
Shenzhen City, China Not on file
SHENZHEN, China Not on file

What they file, and where

Molecule Regulators Docs
Ticagrelor EDQM, US FDA 2
Bivalirudin US FDA 1
Rivaroxaban EDQM 1

Also appears on these molecule pages

Bivalirudin API Ticagrelor API Rivaroxaban API

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) None 1

Questions about Shenzhen Salubris Pharmaceuticals

Does Shenzhen Salubris Pharmaceuticals hold a US DMF or a CEP?
Shenzhen Salubris Pharmaceuticals holds 2 active US drug master files 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 Shenzhen Salubris Pharmaceuticals manufacture?
2 registered sites are on record, in China (Shenzhen City and Shenzhen). Every site is listed on this page with the register it came from.
What does Shenzhen Salubris Pharmaceuticals make?
3 molecules are on record against Shenzhen Salubris Pharmaceuticals, including Ticagrelor, Bivalirudin and Rivaroxaban. Each links through to that molecule's full manufacturer list.
Which regulators recognise Shenzhen Salubris Pharmaceuticals's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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