Suppliers / Shanghai Zhongxi Sunve Pharmaceutical

Shanghai Zhongxi Sunve Pharmaceutical

China Updated 9 July 2026

Shanghai Zhongxi Sunve Pharmaceutical is an API manufacturer based in China. It holds 5 active US drug master files across a filed portfolio of 4 molecules.

5
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
China, China 3002806569

What they file, and where

Molecule Regulators Docs
Hydroxychloroquine US FDA 2
Clozapine US FDA 1
Pyridostigmine US FDA 1
Sulfamethazine US FDA 1

Also appears on these molecule pages

Questions about Shanghai Zhongxi Sunve Pharmaceutical

Does Shanghai Zhongxi Sunve Pharmaceutical hold a US DMF or a CEP?
Shanghai Zhongxi Sunve Pharmaceutical holds 5 active US drug master files. 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.
Is Shanghai Zhongxi Sunve Pharmaceutical FDA-registered?
One site operated by Shanghai Zhongxi Sunve Pharmaceutical carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Shanghai Zhongxi Sunve Pharmaceutical manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does Shanghai Zhongxi Sunve Pharmaceutical make?
4 molecules are on record against Shanghai Zhongxi Sunve Pharmaceutical, including Hydroxychloroquine, Clozapine, Pyridostigmine and Sulfamethazine. 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