Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Germany
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| BK Giulini GmbHRegistrant: BK GIULINI GmbH | Am Hafen 2, Ladenburg, Baden-Wurttemberg 68526, Germany (DEU) | Active ingredient (API) manufacture | 3001347874333732456 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | SODIUM MONOFLUOROPHOSPHATE | powder | 73608-000BULK INGREDIENT |
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Enquiry
Common questions
- Is BK GIULINI GmbH FDA approved?
- BK GIULINI GmbH holds 1 FDA-registered establishment in Germany. 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 BK GIULINI GmbH's drugs manufactured?
- The FDA register lists Ladenburg. Registered operations: active ingredient (API) manufacture.
- What drugs does BK GIULINI GmbH make?
- 1 product is listed under BK GIULINI GmbH 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.