Register entry
Sumitomo Chemical Company, Limited
Data as of · How to read this entry
- Registered sites
- 3
- Active NDC listings
- 8
- Labeller names
- 2
- Live patents
- 0
- Countries
- 1
- Base
- Japan
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture3
Sites
Registered establishments
3| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Sumitomo Chemical Company, Limited | 3750, Azajuhachicho, Maki, Ampachicho, Ampachi-Gun, Gifu 503-0125, Japan (JPN) | Analytical testing, Active ingredient (API) manufacture | 3002808125711530311 |
| Sumitomo Chemical Company, Limited | 6-4-1, Kojimatanokuchi, Kurashiki, Okayama 711-0903, Japan (JPN) | Active ingredient (API) manufacture | 3003973514711530345 |
| Sumitomo Chemical Company, Limited | 2200, Oazatsurusaki, Oita, Oita 870-0106, Japan (JPN) | Active ingredient (API) manufacture | 3002808279695721118 |
Catalogue
Drug listings by form and route
88 active NDC listings: 8 bulk ingredient. By marketing category: BULK INGREDIENT 8.
| Dosage form | NDCs |
|---|---|
| powder | 7 |
| powder, for solution | 1 |
| Route | NDCs |
|---|
| Labeller name on the listing | NDCs |
|---|---|
| sumitomo chemical company, limited | 7 |
| sumitomo chemical co., ltd. | 1 |
Catalogue
Marketed products
8| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Disopyramide Phosphate | powder | 68259-1304BULK INGREDIENT |
| - | Efinaconazole | powder, for solution | 68259-1314BULK INGREDIENT |
| - | Hydralazine Hydrochloride | powder | 68259-1307BULK INGREDIENT |
| - | Hydralazine Hydrochloride | powder | 68259-1313BULK INGREDIENT |
| - | Sofpironium bromide | powder | 68259-1318BULK INGREDIENT |
| - | Vibegron | powder | 68259-1316BULK INGREDIENT |
| - | lurasidone hydrochloride | powder | 68259-1317BULK INGREDIENT |
| - | mirabegron | powder | 68259-1315BULK INGREDIENT |
Neighbours
Registered in the same town
2- Sumika Chemical Analysis Service, Ltd.Oita, JPN
- Sumitomo Pharma Co., Ltd.Oita, JPN
Compare
Comparable companies in Japan
- Chugai Pharmaceutical Co., Ltd.3 sites · 13 NDC
- Daiichi Sankyo Europe GmbH3 sites · 11 NDC
- Meiji Seika Pharma Co., Ltd.3 sites · 1 NDC
- Sumitomo Pharma Co., Ltd.2 sites · 24 NDC
- TAYCA CORPORATION2 sites · 22 NDC
- Shionogi Pharma Co., Ltd.4 sites · 17 NDC
- Terumo Pharmaceutical Services GmbH4 sites · 12 NDC
- Bushu Pharmaceuticals, Ltd.2 sites · 11 NDC
- ASO Pharmaceutical Co. Ltd.2 sites · 10 NDC
- Lead Chemical Co., Ltd.2 sites · 7 NDC
Enquiry
Common questions
- Is Sumitomo Chemical Company, Limited FDA approved?
- Sumitomo Chemical Company, Limited holds 3 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 Sumitomo Chemical Company, Limited's drugs manufactured?
- The FDA register lists Ampachi-Gun; Kurashiki; Oita. Registered operations: analytical testing, active ingredient (API) manufacture.
- What drugs does Sumitomo Chemical Company, Limited make?
- 8 products are listed under Sumitomo Chemical Company, Limited in the openFDA NDC Directory, most often as powder; 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.