Suppliers / Zhejiang Xianfeng Technology Group

Zhejiang Xianfeng Technology Group

China Updated 9 July 2026

Zhejiang Xianfeng Technology Group is an API manufacturer based in China. It holds one active US drug master file.

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

What they file, and where

Molecule Regulators Docs
Macitentan US FDA 1

Also appears on these molecule pages

Macitentan API

Questions about Zhejiang Xianfeng Technology Group

Does Zhejiang Xianfeng Technology Group hold a US DMF or a CEP?
Zhejiang Xianfeng Technology Group holds 1 active US drug master file. 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.
What does Zhejiang Xianfeng Technology Group make?
1 molecule is on record against Zhejiang Xianfeng Technology Group, including Macitentan. 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.

Comparing suppliers?

Choose your molecules and target markets. Zhejiang Xianfeng Technology Group comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Apitoria Pharma shares 1 molecule Alembic Pharmaceuticals shares 1 molecule Matrix Pharmacorp shares 1 molecule Zydus Lifesciences shares 1 molecule Laurus Labs shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability