Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- France
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| K+S FRANCE | ZA SOLVAY PORTE EST ROUTE DES DIGUES, DOMBASLE SUR MEURTHE, MEURTHE-ET-MOSELLE 54110, France (FRA) | Active ingredient (API) manufacture | 3004791302502938033 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | SODIUM CHLORIDE | powder | 69500-110BULK INGREDIENT |
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Enquiry
Common questions
- Is K+S FRANCE FDA approved?
- K+S FRANCE 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 K+S FRANCE's drugs manufactured?
- The FDA register lists DOMBASLE SUR MEURTHE. Registered operations: active ingredient (API) manufacture.
- What drugs does K+S FRANCE make?
- 1 product is listed under K+S FRANCE 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.