Suppliers / Luohe Chief Pharmaceutical

Luohe Chief Pharmaceutical

China Updated 9 July 2026

Luohe Chief Pharmaceutical is a contract manufacturer based in China. It holds 5 active US drug master files and 2 valid CEPs across a filed portfolio of 3 molecules.

5
active US DMFs
2
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
Luohe City, China Not on file
China, China 3017902134

What they file, and where

Molecule Regulators Docs
Rifamycin EDQM, US FDA 4
Rifaximin EDQM, US FDA 2
Rifabutin US FDA 1

Also appears on these molecule pages

Rifamycin contract manufacturing Rifaximin contract manufacturing

Questions about Luohe Chief Pharmaceutical

Does Luohe Chief Pharmaceutical hold a US DMF or a CEP?
Luohe Chief Pharmaceutical holds 5 active US drug master files and 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.
Is Luohe Chief Pharmaceutical FDA-registered?
One site operated by Luohe Chief 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 Luohe Chief Pharmaceutical manufacture?
2 registered sites are on record, in China (Luohe City and China). Every site is listed on this page with the register it came from.
What does Luohe Chief Pharmaceutical make?
3 molecules are on record against Luohe Chief Pharmaceutical, including Rifamycin, Rifaximin and Rifabutin. 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