Suppliers / Curia Italy

Curia Italy

Italy Updated 9 July 2026

The public registers hold a second record for Curia Italy. The fuller profile, with 116 active US DMFs and 8 valid CEPs, is at Curia. Figures on this page cover only this record.

Curia Italy is an API manufacturer based in Italy. It holds 29 active US drug master files across a filed portfolio of 23 molecules.

29
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Aztreonam US FDA 3
(21R)-Argatroban US FDA 2
Cyclosporine US FDA 2
Mecamylamine US FDA 2
Minocycline US FDA 2
Azelastine US FDA 1
Bromocriptine US FDA 1
Chlorthalidone US FDA 1
Desogestrel US FDA 1
Dihydroergotamine US FDA 1
Show all 23 molecules on file
Ergotamine US FDA 1
Flutamide US FDA 1
Monomethyl Fumarate US FDA 1
Mycophenolic Acid US FDA 1
Oxandrolone US FDA 1
Pancuronium US FDA 1
Pimecrolimus US FDA 1
Propofol US FDA 1
Ribavirin US FDA 1
Rocuronium US FDA 1
Sirolimus US FDA 1
Ticlopidine US FDA 1
Vecuronium US FDA 1

Also appears on these molecule pages

Show 2 more molecule pages

Questions about Curia Italy

Does Curia Italy hold a US DMF or a CEP?
Curia Italy holds 29 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.
What does Curia Italy make?
23 molecules are on record against Curia Italy, including Aztreonam, (21R)-Argatroban, Cyclosporine and Mecamylamine. Each links through to that molecule's full manufacturer list.

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

  • 1 active litigation matter is on record.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability