Is Suanfarma Italia SpA FDA approved?

Suanfarma Italia SpA holds 1 FDA-registered establishment 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 Suanfarma Italia SpA's drugs manufactured?

The FDA register lists Rovereto Trentino. Registered operations: analytical testing, active ingredient (API) manufacture.

What drugs does Suanfarma Italia SpA make?

1 product is listed under Suanfarma Italia SpA 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.

Suanfarma Italia SpA

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

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Registered sites: 1
Active NDC listings: 1
Live patents: 0
Countries: 1
Base: Italy

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Suanfarma Italia S.p.A.Registrant: Suanfarma Italia SpA	Corso Verona 165, Rovereto Trentino, - 38068, Italy (ITA)	Analytical testing, Active ingredient (API) manufacture	1000312133429636954

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Tiamulin Hydrogen Fumarate	powder	55073-0400BULK INGREDIENT

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Enquiry

Common questions

Is Suanfarma Italia SpA FDA approved?: Suanfarma Italia SpA holds 1 FDA-registered establishment 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 Suanfarma Italia SpA's drugs manufactured?: The FDA register lists Rovereto Trentino. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does Suanfarma Italia SpA make?: 1 product is listed under Suanfarma Italia SpA 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.