Suppliers / Angelini Pharma

Angelini Pharma

Italy Updated 9 July 2026

Angelini Pharma is an API and finished-dose manufacturer based in Italy. It holds one active US drug master file. Its filings concentrate with AEMPS (ES), EMA and SWISSMEDIC (CH).

1
active US DMFs
0
valid CEPs
1
registered plants
149
filings across 11 regulators

Registered plants

Site FDA FEI
Zug, Switzerland Not on file

What they file, and where

Molecule Regulators Docs
Trazodone US FDA 1

Also appears on these molecule pages

Capsaicin finished dose Cenobamate finished dose Dalbavancin finished dose Lurasidone finished dose Trazodone API

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) 53 None
EMA 28 None
SWISSMEDIC (CH) 13 None
MPA (SE) 12 None
AIFA (IT) 11 None
DKMA (DK) 9 None

Questions about Angelini Pharma

Does Angelini Pharma hold a US DMF or a CEP?
Angelini Pharma holds 1 active US drug master file. 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.
Where does Angelini Pharma manufacture?
1 registered site is on record, in Switzerland (Zug). Every site is listed on this page with the register it came from.
What does Angelini Pharma make?
1 molecule is on record against Angelini Pharma, including Trazodone. Each links through to that molecule's full manufacturer list.
Where does Angelini Pharma file?
Filings are on record with AEMPS (ES), EMA, SWISSMEDIC (CH), MPA (SE) and 7 other regulators, 149 in total.

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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Sources on this page

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