Suppliers / Shanghai Desano Chemical Pharmaceutical

Shanghai Desano Chemical Pharmaceutical

China Updated 9 July 2026

Shanghai Desano Chemical Pharmaceutical is an API manufacturer based in China. It holds 32 active US drug master files and 10 valid CEPs. Its GMP standing is certified by MHRA (UK) and US FDA. Its most recent recorded inspection, by US FDA, closed on 17 November 2023 as VAI.

32
active US DMFs
10
valid CEPs
3
registered plants 1 with an FDA FEI number
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 17 November 2023 VAI US FDA
  • 10 March 2017 VAI US FDA
  • 7 May 2015 OAI US FDA
  • 7 June 2012 NAI US FDA
  • 24 April 2009 VAI US FDA

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

Registered plants

Site FDA FEI
Laogang Town, China Not on file
SHANGHAI, China Not on file
China, China 3006895951

What they file, and where

Molecule Regulators Docs
Lamivudine EDQM, US FDA 3
Ritonavir EDQM, US FDA 3
Atazanavir EDQM, US FDA 2
Lopinavir US FDA 2
Nevirapine EDQM, US FDA 2
Praziquantel EDQM, US FDA 2
Zidovudine EDQM, US FDA 2
Abacavir EDQM 1
Atovaquone US FDA 1
Cabotegravir US FDA 1
Show all 30 molecules on file
Canagliflozin US FDA 1
Dolutegravir US FDA 1
Dotinurad US FDA 1
Edoxaban US FDA 1
Efavirenz US FDA 1
Elagolix US FDA 1
Eltrombopag US FDA 1
Elvitegravir US FDA 1
Emtricitabine US FDA 1
Finerenone US FDA 1
Isavuconazonium US FDA 1
Lasmiditan US FDA 1
Letermovir US FDA 1
Lumefantrine US FDA 1
Omadacycline US FDA 1
Oseltamivir US FDA 1
Raltegravir EDQM 1
Rilpivirine US FDA 1
Rosuvastatin US FDA 1
Tedizolid US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
BOMRA (BW) 1 None
MHRA (UK) None 3
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 17 November 2023.

Sources on this page

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