Suppliers / Qilu Synva Pharmaceutical

Qilu Synva Pharmaceutical

China Updated 9 July 2026

The public registers hold a second record for Qilu Synva Pharmaceutical. The fuller profile, with 31 active US DMFs and 12 valid CEPs, is at Qilu Pharmaceutical. Figures on this page cover only this record.

Qilu Synva Pharmaceutical is an API manufacturer based in China. It holds one valid CEP.

0
active US DMFs
1
valid CEPs
2
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
Dezhou, China Not on file
China, China 3006385404

What they file, and where

Molecule Regulators Docs
Flunixin Meglumine For Veterinary Use EDQM 1

Also appears on these molecule pages

Flunixin Meglumine For Veterinary Use API

Questions about Qilu Synva Pharmaceutical

Does Qilu Synva Pharmaceutical hold a US DMF or a CEP?
Qilu Synva 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.
Is Qilu Synva Pharmaceutical FDA-registered?
One site operated by Qilu Synva 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 Qilu Synva Pharmaceutical manufacture?
2 registered sites are on record, in China (Dezhou and China). Every site is listed on this page with the register it came from.
What does Qilu Synva Pharmaceutical make?
1 molecule is on record against Qilu Synva Pharmaceutical, including Flunixin Meglumine For Veterinary Use. 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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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