Suppliers / Minsheng Group Shaoxing Pharmaceutical

Minsheng Group Shaoxing Pharmaceutical

China Updated 9 July 2026

Minsheng Group Shaoxing Pharmaceutical is an API manufacturer based in China. It holds 4 active US drug master files across a filed portfolio of 4 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 15 November 2024 as VAI.

4
active US DMFs
0
valid CEPs
1
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
Inspections
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 15 November 2024 VAI US FDA
  • 25 January 2019 NAI US FDA
  • 14 April 2017 VAI US FDA
  • 27 May 2010 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
China, China 3004986788

What they file, and where

Molecule Regulators Docs
Alendronic Acid US FDA 1
Atropine US FDA 1
Nitrofurazone US FDA 1
Omacetaxine Mepesuccinate US FDA 1

Also appears on these molecule pages

Alendronic Acid API Atropine API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Minsheng Group Shaoxing Pharmaceutical

Does Minsheng Group Shaoxing Pharmaceutical hold a US DMF or a CEP?
Minsheng Group Shaoxing Pharmaceutical holds 4 active US drug master files. 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 Minsheng Group Shaoxing Pharmaceutical FDA-registered?
One site operated by Minsheng Group Shaoxing 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.
How did Minsheng Group Shaoxing Pharmaceutical's last inspection go?
The most recent inspection on record closed on 15 November 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 4 inspections are on file.
Where does Minsheng Group Shaoxing Pharmaceutical manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does Minsheng Group Shaoxing Pharmaceutical make?
4 molecules are on record against Minsheng Group Shaoxing Pharmaceutical, including Alendronic Acid, Atropine, Nitrofurazone and Omacetaxine Mepesuccinate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Minsheng Group Shaoxing Pharmaceutical's GMP?
Current GMP certificates are on record from US FDA. 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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Open risk flags

  • The most recent inspection outcome was VAI, on 15 November 2024.

Comparable suppliers

Matrix Pharmacorp shares 2 molecules Apitoria Pharma shares 1 molecule Cipla shares 1 molecule Dr Reddy's Laboratories shares 1 molecule Ipca Laboratories shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates