Register entry

SERIPHARM

Data as of · How to read this entry

Registered sites
1
Active NDC listings
3
Labeller names
2
Live patents
0
Countries
1
Base
France
Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
SERIPHARM1 RUE DEMOCRITE, Le Mans, 72000, France (FRA)Analytical testing, Active ingredient (API) manufacture3002808119775749484
Catalogue

Drug listings by form and route

3

3 active NDC listings: 3 bulk ingredient. By marketing category: BULK INGREDIENT 3.

Dosage formNDCs
powder3
RouteNDCs
Labeller name on the listingNDCs
seripharm2
seripharm s.a.s.1
Catalogue

Marketed products

3
BrandGeneric nameForm / routeNDC
-PACLITAXELpowder62422-0001BULK INGREDIENT
-PACLITAXELpowder62422-0002BULK INGREDIENT
-PACLITAXELpowder62422-0004BULK INGREDIENT
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Comparable companies in France

Enquiry

Common questions

Is SERIPHARM FDA approved?
SERIPHARM holds 1 FDA-registered establishment in France. 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 SERIPHARM's drugs manufactured?
The FDA register lists Le Mans. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does SERIPHARM make?
3 products are listed under SERIPHARM 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.