Is Lusochimica SPA FDA approved?

Lusochimica SPA 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 Lusochimica SPA's drugs manufactured?

The FDA register lists Lomagna; Pisa. Registered operations: analytical testing, active ingredient (API) manufacture.

What drugs does Lusochimica SPA make?

13 products are listed under Lusochimica 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.

Lusochimica SPA

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

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Registered sites: 2
Active NDC listings: 13
Labeller names: 2
Live patents: 0
Countries: 1
Base: Italy

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Lusochimica SpA	Via Giotto 9, Lomagna, 23871, Italy (ITA)	Active ingredient (API) manufacture	3002807514428179048
Lusochimica SPA	Via Livornese 897, Pisa, 56122, Italy (ITA)	Analytical testing	3002807437338628901

Catalogue

Drug listings by form and route

13 active NDC listings: 13 bulk ingredient. By marketing category: BULK INGREDIENT 13.

Dosage form	NDCs
powder	13

Route	NDCs

Labeller name on the listing	NDCs
lusochimica spa	10
lusochimica spa	3

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Albuterol Sulfate	powder	43898-0123BULK INGREDIENT
-	Albuterol Sulfate	powder	43898-0133BULK INGREDIENT
-	Carteolol Hydrochloride	powder	43898-0104BULK INGREDIENT
-	Formoterol Fumarate Dihydrate	powder	43898-0130BULK INGREDIENT
-	Formoterol Fumarate Dihydrate	powder	43898-0131BULK INGREDIENT
-	Ipratropium Bromide	powder	43898-0102BULK INGREDIENT
-	Ipratropium Bromide	powder	43898-0135BULK INGREDIENT
-	Metaproterenol Sulfate	powder	43898-0106BULK INGREDIENT
-	Nicardipine Hydrochloride	powder	43898-0103BULK INGREDIENT
-	Nicardipine Hydrochloride	powder	43898-0124BULK INGREDIENT
-	Nimodipine	powder	43898-0117BULK INGREDIENT
-	Silver Sulfadiazine	powder	43898-0134BULK INGREDIENT
-	Tolnaftate	powder	43898-0136BULK INGREDIENT

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
Doppel Farmaceutici S.r.l.2 sites · 10 NDC
Trifarma S.p.A.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 Lusochimica SPA FDA approved?: Lusochimica SPA 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 Lusochimica SPA's drugs manufactured?: The FDA register lists Lomagna; Pisa. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does Lusochimica SPA make?: 13 products are listed under Lusochimica 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.