Suppliers / Zhejiang Charioteer Pharmaceutical

Zhejiang Charioteer Pharmaceutical

China Updated 9 July 2026

Zhejiang Charioteer Pharmaceutical is a contract manufacturer based in China. It holds 11 active US drug master files across a filed portfolio of 9 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 8 November 2024 as NAI.

11
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

  • 8 November 2024 NAI US FDA
  • 18 January 2018 VAI US FDA
  • 4 July 2014 VAI US FDA
  • 15 September 2011 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 3002808516

What they file, and where

Molecule Regulators Docs
Naproxen SFDA (Saudi Arabia), US FDA 4
Acyclovir SFDA (Saudi Arabia), US FDA 2
Clopidogrel SFDA (Saudi Arabia), US FDA 2
Adefovir US FDA 1
Famciclovir US FDA 1
Letermovir US FDA 1
Penciclovir US FDA 1
Valaciclovir US FDA 1
Valganciclovir US FDA 1

Also appears on these molecule pages

Acyclovir contract manufacturing Clopidogrel contract manufacturing Ketorolac Tromethamine contract manufacturing Naproxen contract manufacturing Valaciclovir contract manufacturing Valacyclovir contract manufacturing

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was NAI, on 8 November 2024.

Sources on this page

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