Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- France
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1Labelling1Packaging1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| V. MANE FILS | MANE 620 ROUTE DE GRASSE, LE BAR SUR LOUP, ALPES-MARITIMES 06620, France (FRA) | Analytical testing, Active ingredient (API) manufacture, Labelling, Packaging | 3004334539274581214 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Thymol | crystal | 72702-002BULK INGREDIENT |
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Enquiry
Common questions
- Is V. MANE FILS FDA approved?
- V. MANE FILS 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 V. MANE FILS's drugs manufactured?
- The FDA register lists LE BAR SUR LOUP. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, packaging.
- What drugs does V. MANE FILS make?
- 1 product is listed under V. MANE FILS in the openFDA NDC Directory, most often as crystal. 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.