Register entry

Sumitomo Chemical Company, Limited

Registered sites
3
Drug products
8
Live patents
0
Countries
1
Base
Japan
Authorisation

Registered operations

What the FDA has registered these sites to do. This is the regulatory record, not a marketing claim.

Analytical testingActive ingredient (API) manufacture
Sites

Facilities

3
SiteLocationOperationsFEI
Sumitomo Chemical Company, LimitedAmpachi-GunJapanAnalytical testing, Active ingredient (API) manufacture3002808125
Sumitomo Chemical Company, LimitedKurashikiJapanActive ingredient (API) manufacture3003973514
Sumitomo Chemical Company, LimitedOitaJapanActive ingredient (API) manufacture3002808279
Catalogue

Marketed products

8

Showing 8 of 8.

BrandGeneric nameFormCategory
-Disopyramide PhosphatePOWDERBULK INGREDIENT
-EfinaconazolePOWDER, FOR SOLUTIONBULK INGREDIENT
-Hydralazine HydrochloridePOWDERBULK INGREDIENT
-Hydralazine HydrochloridePOWDERBULK INGREDIENT
-Sofpironium bromidePOWDERBULK INGREDIENT
-VibegronPOWDERBULK INGREDIENT
-lurasidone hydrochloridePOWDERBULK INGREDIENT
-mirabegronPOWDERBULK INGREDIENT
Provenance

Facility and operations data from the FDA Drug Establishments Current Registration Site. Product data from the openFDA National Drug Code Directory. Patent and exclusivity data from the FDA Orange Book. Shortage data from the FDA drug shortage database. Contact details the FDA publishes for registered establishments are deliberately not reproduced here. This entry is compiled from public records and has not been claimed by the company.