Suppliers / Wuhan Wuyao Pharmaceutical

Wuhan Wuyao Pharmaceutical

China Updated 9 July 2026

Wuhan Wuyao Pharmaceutical is an API manufacturer based in China. It holds 12 valid CEPs across a filed portfolio of 11 molecules. Its GMP standing is certified by EMA and US FDA. Its most recent recorded inspection, by US FDA, closed on 7 March 2025 as VAI.

0
active US DMFs
12
valid CEPs
3
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
3 of 3 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 7 March 2025 VAI US FDA
  • 9 March 2018 NAI US FDA
  • 13 May 2016 VAI US FDA

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

Registered plants

Site FDA FEI
Huangshi, China Not on file
Huangshi City, China Not on file
China, China 3010686159

What they file, and where

Molecule Regulators Docs
Norepinephrine EDQM, SFDA (Saudi Arabia) 3
Epinephrine EDQM 2
Metronidazole EDQM 2
Dopamine EDQM 1
Hydroxychloroquine EDQM 1
Isoprenaline EDQM 1
Metamizole EDQM 1
Norepinephrine Bitartrate SFDA (Saudi Arabia) 1
Phenylephrine EDQM 1
Trimetazidine Dihydrochloride EDQM 1
Show all 11 molecules on file
Xylometazoline EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 7 March 2025.

Sources on this page

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