Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Japan
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| SHIONO FINESSE, LTD.Registrant: Shiono Finesse Ltd. | 49HAMAWARI156-1, MIKUNICHOYONOZU, SAKAI, FUKUI 913-0036, Japan (JPN) | Active ingredient (API) manufacture | 3005940219713886984 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Silodosin | powder | 42334-001BULK INGREDIENT |
Compare
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Enquiry
Common questions
- Is Shiono Finesse Ltd. FDA approved?
- Shiono Finesse Ltd. holds 1 FDA-registered establishment in Japan. 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 Shiono Finesse Ltd.'s drugs manufactured?
- The FDA register lists SAKAI. Registered operations: active ingredient (API) manufacture.
- What drugs does Shiono Finesse Ltd. make?
- 1 product is listed under Shiono Finesse Ltd. 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.