Suppliers / Chifeng Arker Pharmaceutical Technology

Chifeng Arker Pharmaceutical Technology

China Updated 9 July 2026

Chifeng Arker Pharmaceutical Technology is an API manufacturer based in China. It holds 2 valid CEPs across a filed portfolio of 2 molecules.

0
active US DMFs
2
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Chifeng, China Not on file

What they file, and where

Molecule Regulators Docs
Dextromethorphan EDQM 1
Pseudoephedrine EDQM 1

Also appears on these molecule pages

Dextromethorphan API Pseudoephedrine API

Questions about Chifeng Arker Pharmaceutical Technology

Does Chifeng Arker Pharmaceutical Technology hold a US DMF or a CEP?
Chifeng Arker Pharmaceutical Technology holds 2 valid CEPs. 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 Chifeng Arker Pharmaceutical Technology manufacture?
1 registered site is on record, in China (Chifeng). Every site is listed on this page with the register it came from.
What does Chifeng Arker Pharmaceutical Technology make?
2 molecules are on record against Chifeng Arker Pharmaceutical Technology, including Dextromethorphan and Pseudoephedrine. 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. Chifeng Arker Pharmaceutical Technology comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Malladi Drugs & Pharmaceuticals shares 2 molecules Zhejiang Apeloa Kangyu Pharmaceutical shares 2 molecules Far Specialty Products Inc Dba Far Chemical shares 2 molecules Apitoria Pharma shares 1 molecule Siegfried 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