Is Trifarma S.p.A. FDA approved?

Trifarma S.p.A. holds 2 FDA-registered establishments in Italy. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Trifarma S.p.A.'s drugs manufactured?

The FDA register lists CERIANO LAGHETTO; Rozzano. Registered operations: analytical testing, active ingredient (API) manufacture.

What drugs does Trifarma S.p.A. make?

10 products are listed under Trifarma S.p.A. in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Trifarma S.p.A.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 2
Active NDC listings: 10
Labeller names: 2
Live patents: 0
Countries: 1
Base: Italy

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture2

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Trifarma S.p.ARegistrant: Trifarma S.p.A.	VIA DELL'INDUSTRIA 6, CERIANO LAGHETTO, 20816, Italy (ITA)	Active ingredient (API) manufacture	1000532829435904107
Trifarma S.p.A.	Via Pavese 2, Rozzano, 20089, Italy (ITA)	Analytical testing, Active ingredient (API) manufacture	3002807260447104712

Catalogue

Drug listings by form and route

10 active NDC listings: 10 bulk ingredient. By marketing category: BULK INGREDIENT 10.

Dosage form	NDCs
powder	10

Route	NDCs

Labeller name on the listing	NDCs
trifarma s.p.a	8
trifarma s.p.a.	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Clindamycin Phosphate	powder	46204-0120BULK INGREDIENT
-	Fluphenazine Hydrochloride	powder	46204-0002BULK INGREDIENT
-	Halobetasol Propionate	powder	46204-0188BULK INGREDIENT
-	Minoxidil	powder	46204-0159BULK INGREDIENT
-	Perphenazine	powder	46204-0003BULK INGREDIENT
-	Prochlorperazine	powder	46204-0007BULK INGREDIENT
-	Prochlorperazine Edisylate	powder	46204-0121BULK INGREDIENT
-	Prochlorperazine Maleate	powder	46204-0106BULK INGREDIENT
-	Testosterone Cypionate	powder	46204-0371BULK INGREDIENT
-	Thioridazine Hydrochloride	powder	46204-0006BULK INGREDIENT

Neighbours

Registered in the same town

Curia India Private LimitedROZZANO, ITA; Rozzano, ITA · 2 sites
BRACCO DIAGNOSTICS INCCeriano Laghetto, ITA

Compare

Comparable companies in Italy

Erregierre SpA2 sites · 36 NDC
Newchem S.p.A.2 sites · 33 NDC
Novo Nordisk Production Belgium SA2 sites · 24 NDC
Indena SpA2 sites · 15 NDC
Italfarmaco S.A.2 sites · 15 NDC
Lusochimica SPA2 sites · 13 NDC
Doppel Farmaceutici S.r.l.2 sites · 10 NDC
CHEMI SpA2 sites · 4 NDC
OPOCRIN SPA2 sites · 2 NDC
AMSA Anonima Materie Sintetiche ED Affini Spa2 sites · 0 NDC

Enquiry

Common questions

Is Trifarma S.p.A. FDA approved?: Trifarma S.p.A. holds 2 FDA-registered establishments in Italy. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Trifarma S.p.A.'s drugs manufactured?: The FDA register lists CERIANO LAGHETTO; Rozzano. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does Trifarma S.p.A. make?: 10 products are listed under Trifarma S.p.A. in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.