Suppliers / Hec Api Yichang

Hec Api Yichang

China Updated 9 July 2026

The public registers hold a second record for Hec Api Yichang. The fuller profile, with 43 active US DMFs and 4 valid CEPs, is at HEC Pharm. Figures on this page cover only this record.

Hec Api Yichang is an API manufacturer based in China. It holds one active US drug master file and one valid CEP across a filed portfolio of 2 molecules.

1
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
Yidu City, China Not on file
China, China 3018718574

What they file, and where

Molecule Regulators Docs
Finerenone US FDA 1
Moxifloxacin Hydrochloride EDQM 1

Also appears on these molecule pages

Questions about Hec Api Yichang

Does Hec Api Yichang hold a US DMF or a CEP?
Hec Api Yichang holds 1 active US drug master file and 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 Hec Api Yichang FDA-registered?
One site operated by Hec Api Yichang 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 Hec Api Yichang manufacture?
2 registered sites are on record, in China (Yidu City and China). Every site is listed on this page with the register it came from.
What does Hec Api Yichang make?
2 molecules are on record against Hec Api Yichang, including Finerenone and Moxifloxacin Hydrochloride. 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