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

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) None 1

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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