Suppliers / Ningbo Menovo Pharmaceutical

Ningbo Menovo Pharmaceutical

China 41 employees Updated 9 July 2026

Ningbo Menovo Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file and 11 valid CEPs across a filed portfolio of 7 molecules.

1
active US DMFs
11
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Ningbo, China Not on file
Ningbo Hi-Tech District, China Not on file

What they file, and where

Molecule Regulators Docs
Rosuvastatin EDQM, US FDA 4
Atorvastatin EDQM 2
Esomeprazole EDQM 2
Fipronil For Veterinary Use EDQM 1
Losartan Potassium EDQM 1
Perindopril Tert-Butylamine EDQM 1
Valsartan EDQM 1

Also appears on these molecule pages

Questions about Ningbo Menovo Pharmaceutical

Does Ningbo Menovo Pharmaceutical hold a US DMF or a CEP?
Ningbo Menovo Pharmaceutical holds 1 active US drug master file and 11 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.
Where does Ningbo Menovo Pharmaceutical manufacture?
2 registered sites are on record, in China (Ningbo and Ningbo Hi-tech District). Every site is listed on this page with the register it came from.
What does Ningbo Menovo Pharmaceutical make?
7 molecules are on record against Ningbo Menovo Pharmaceutical, including Rosuvastatin, Atorvastatin, Esomeprazole and Fipronil 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability