Suppliers / Zhejiang Menovo Pharmaceutical

Zhejiang Menovo Pharmaceutical

China Updated 9 July 2026

Zhejiang Menovo Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file across a filed portfolio of 3 molecules. Its GMP standing is certified by EMA.

1
active US DMFs
0
valid CEPs
2
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Shangyu, China Not on file
Shangyu City, China Not on file

What they file, and where

Molecule Regulators Docs
Levocetirizine Dihydrochloride SFDA (Saudi Arabia) 1
Perindopril Erbumine SFDA (Saudi Arabia) 1
Rosuvastatin US FDA 1

Also appears on these molecule pages

Levocetirizine API Rosuvastatin API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1

Questions about Zhejiang Menovo Pharmaceutical

Does Zhejiang Menovo Pharmaceutical hold a US DMF or a CEP?
Zhejiang Menovo Pharmaceutical holds 1 active US drug master file. 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 Zhejiang Menovo Pharmaceutical manufacture?
2 registered sites are on record, in China (Shangyu and Shangyu City). Every site is listed on this page with the register it came from.
What does Zhejiang Menovo Pharmaceutical make?
3 molecules are on record against Zhejiang Menovo Pharmaceutical, including Levocetirizine Dihydrochloride, Perindopril Erbumine and Rosuvastatin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Zhejiang Menovo Pharmaceutical's GMP?
Current GMP certificates are on record from EMA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates