Suppliers / Chengdu Runde Pharmaceutical

Chengdu Runde Pharmaceutical

China 2 employees Updated 9 July 2026

Chengdu Runde Pharmaceutical is an API manufacturer based in China. It holds one valid CEP.

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

Registered plants

Site FDA FEI
Chengdu, China Not on file

What they file, and where

Molecule Regulators Docs
Diosmin EDQM 1

Also appears on these molecule pages

Diosmin API

Questions about Chengdu Runde Pharmaceutical

Does Chengdu Runde Pharmaceutical hold a US DMF or a CEP?
Chengdu Runde Pharmaceutical holds 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 Chengdu Runde Pharmaceutical manufacture?
1 registered site is on record, in China (Chengdu). Every site is listed on this page with the register it came from.
What does Chengdu Runde Pharmaceutical make?
1 molecule is on record against Chengdu Runde Pharmaceutical, including Diosmin. 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. Chengdu Runde Pharmaceutical comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

PMC Isochem shares 1 molecule Interquim shares 1 molecule Sichuan Xieli Pharmaceutical shares 1 molecule Healthtech Bioactives Slu shares 1 molecule Sichuan New Hawk Biotechnology Co.,Ltd 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