Suppliers / Tianjin Tasly Sants Pharmaceutical

Tianjin Tasly Sants Pharmaceutical

China Updated 9 July 2026

Tianjin Tasly Sants Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file. Its GMP standing is certified by EMA and MHRA (UK).

1
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
TIANJIN, China Not on file

What they file, and where

Molecule Regulators Docs
Eszopiclone US FDA 1

Also appears on these molecule pages

Eszopiclone API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1
MHRA (UK) 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