Suppliers / Zhejiang NHU

Zhejiang NHU

China Updated 9 July 2026

Zhejiang NHU 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
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
Shaoxing City, China Not on file
China, China 3004347352

What they file, and where

Molecule Regulators Docs
Ibuprofen EDQM 1
Moxifloxacin EDQM 1

Also appears on these molecule pages

Ibuprofen API Moxifloxacin API

Questions about Zhejiang NHU

Does Zhejiang NHU hold a US DMF or a CEP?
Zhejiang NHU 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.
Is Zhejiang NHU FDA-registered?
One site operated by Zhejiang NHU 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 Zhejiang NHU manufacture?
2 registered sites are on record, in China (Shaoxing City and China). Every site is listed on this page with the register it came from.
What does Zhejiang NHU make?
2 molecules are on record against Zhejiang NHU, including Ibuprofen and Moxifloxacin. 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