Suppliers / Sichuan Gowell Pharmaceutical

Sichuan Gowell Pharmaceutical

China Updated 9 July 2026

Sichuan Gowell Pharmaceutical is an API manufacturer based in China. It holds 6 active US drug master files and one valid CEP across a filed portfolio of 6 molecules.

6
active US DMFs
1
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Meishan City, China Not on file

What they file, and where

Molecule Regulators Docs
Icosapent Ethyl US FDA 2
Iron Sucrose US FDA 1
Nusinersen US FDA 1
Omega-3-Acid Ethyl Esters 90 EDQM 1
Sodium Zirconium Cyclosilicate US FDA 1
Upadacitinib US FDA 1

Also appears on these molecule pages

Icosapent Ethyl API Nusinersen API Sodium Zirconium Cyclosilicate API Upadacitinib API

Questions about Sichuan Gowell Pharmaceutical

Does Sichuan Gowell Pharmaceutical hold a US DMF or a CEP?
Sichuan Gowell Pharmaceutical holds 6 active US drug master files and 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 Sichuan Gowell Pharmaceutical manufacture?
1 registered site is on record, in China (Meishan City). Every site is listed on this page with the register it came from.
What does Sichuan Gowell Pharmaceutical make?
6 molecules are on record against Sichuan Gowell Pharmaceutical, including Icosapent Ethyl, Iron Sucrose, Nusinersen and Omega-3-Acid Ethyl Esters 90. 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