Register entry
- Registered sites
- 2
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Japan
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture2
Sites
Registered establishments
2| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| UBE Corporation | 955 Koiwai, Yoshitomimachi, Chikujo-gun, Fukuoka 871-0801, Japan (JPN) | Active ingredient (API) manufacture | 3002808530739192231 |
| UBE Corporation | 1978-10, Kogushi, Ube, Yamaguchi 755-8633, Japan (JPN) | Analytical testing, Active ingredient (API) manufacture | 3003604942695266288 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Bepotastine | powder | 42672-0100BULK INGREDIENT |
Neighbours
Registered in the same town
2- Central Glass CO., LTD.UBE, JPN
- Titan Kogyo , Ltd.UBE, JPN
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Enquiry
Common questions
- Is UBE Corporation FDA approved?
- UBE Corporation holds 2 FDA-registered establishments 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 UBE Corporation's drugs manufactured?
- The FDA register lists Chikujo-gun; Ube. Registered operations: analytical testing, active ingredient (API) manufacture.
- What drugs does UBE Corporation make?
- 1 product is listed under UBE Corporation 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.