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 |
|---|---|---|---|
| Kaneka Corporation | 1-8, TakasagochoMiyamaecho, Takasago, Hyogo 6760027, Japan (JPN) | Active ingredient (API) manufacture | 3002807368695780510 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | EFINACONAZOLE | powder, for solution | 84678-001BULK INGREDIENT |
Compare
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Enquiry
Common questions
- Is Kaneka Corporation FDA approved?
- Kaneka Corporation 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 Kaneka Corporation's drugs manufactured?
- The FDA register lists Takasago. Registered operations: active ingredient (API) manufacture.
- What drugs does Kaneka Corporation make?
- 1 product is listed under Kaneka Corporation in the openFDA NDC Directory, most often as powder, for solution. 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.