Register entry

Danipharm A/S

Data as of · How to read this entry

Registered sites
1
Active NDC listings
1
Live patents
0
Countries
1
Base
Denmark
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Danipharm A/SSkalhuse 3, NIBE, 9240, Denmark (DNK)Active ingredient (API) manufacture3002806781310631791
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-Lactuloseliquid50065-000BULK INGREDIENT
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Common questions

Is Danipharm A/S FDA approved?
Danipharm A/S holds 1 FDA-registered establishment in Denmark. 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 Danipharm A/S's drugs manufactured?
The FDA register lists NIBE. Registered operations: active ingredient (API) manufacture.
What drugs does Danipharm A/S make?
1 product is listed under Danipharm A/S in the openFDA NDC Directory, most often as liquid. 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.