Suppliers / Corden Pharma

Corden Pharma

Italy 3 duplicate records merged Updated 9 July 2026

Corden Pharma is a finished-dose manufacturer based in Italy. It holds one active US drug master file. Its filings concentrate with US FDA, MINSA (CR) and ARCSA (EC). Its GMP standing is certified by EMA, ZLG (DE) and US FDA. Its most recent recorded inspection, by US FDA, closed on 14 June 2024 as VAI. Customs aggregates show $37K of exports covering 10 molecules to 1 destination in 2022.

1
active US DMFs
0
valid CEPs
7
registered plants 2 with an FDA FEI number
24
filings across 9 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
4 of 4 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

  • 14 June 2024 VAI US FDA
  • 2 November 2018 NAI US FDA
  • 31 January 2014 NAI US FDA
  • 22 December 2011 VAI US FDA

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

Registered plants

Site FDA FEI
Plankstadt, United Arab Emirates Not on file
Caponago, United Arab Emirates Not on file
Switzerland, Switzerland 3002561809
Frankfurt, Germany Not on file
Germany, Germany 3012722976
CAPONAGO, Italy Not on file

1 further sites are on record.

What they file, and where

Molecule Regulators Docs
1 US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 8 1
MINSA (CR) 4 None
ARCSA (EC) 3 None
INVIMA (CO) 2 None
NAFDAC (NG) 2 None
DIGEMAPS (DO) 2 None
EMA None 4
ZLG (DE) None 4

Scale

Year Revenue Exports Destinations
2022 Not reported $37K 1

Export figures are customs aggregates. We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was VAI, on 14 June 2024.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts