Register entry

UBE Corporation

Data as of · How to read this 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
EstablishmentAddressRegistered forFEI / DUNS
UBE Corporation955 Koiwai, Yoshitomimachi, Chikujo-gun, Fukuoka 871-0801, Japan (JPN)Active ingredient (API) manufacture3002808530739192231
UBE Corporation1978-10, Kogushi, Ube, Yamaguchi 755-8633, Japan (JPN)Analytical testing, Active ingredient (API) manufacture3003604942695266288
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-Bepotastinepowder42672-0100BULK INGREDIENT
Neighbours

Registered in the same town

2
Compare

Comparable companies in Japan

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.