Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Italy
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Latina Pharma S.P.ARegistrant: Latina Pharma S.P.A. | Via Murillo, 7, Sermoneta, Latina 04013, Italy (ITA) | Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging | 3001229385339062883 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | AZTREONAM | powder | 61126-710BULK INGREDIENT |
Neighbours
Registered in the same town
1- Biosint S.p.ASermoneta, ITA
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Enquiry
Common questions
- Is Latina Pharma S.P.A. FDA approved?
- Latina Pharma S.P.A. 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 Latina Pharma S.P.A.'s drugs manufactured?
- The FDA register lists Sermoneta. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
- What drugs does Latina Pharma S.P.A. make?
- 1 product is listed under Latina Pharma 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.