Register entry

Shiratori Pharmaceutical Co., Ltd.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
2
Live patents
0
Countries
1
Base
Japan
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Shiratori Pharmaceutical Co., Ltd.54, Shimminato, Mihama-Ku, Chiba, Chiba, 261-0002, Japan (JPN)Active ingredient (API) manufacture3002808233716664227
Catalogue

Drug listings by form and route

2

2 active NDC listings: 2 bulk ingredient. By marketing category: BULK INGREDIENT 2.

Dosage formNDCs
powder2
RouteNDCs
Labeller name on the listingNDCs
shiratori pharmaceutical co., ltd.2
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
-EMEDASTINE DIFUMARATEpowder12863-100BULK INGREDIENT
-SAPROPTERIN DIHYDROCHLORIDEpowder12863-110BULK INGREDIENT
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Comparable companies in Japan

Enquiry

Common questions

Is Shiratori Pharmaceutical Co., Ltd. FDA approved?
Shiratori Pharmaceutical Co., Ltd. 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 Shiratori Pharmaceutical Co., Ltd.'s drugs manufactured?
The FDA register lists Chiba. Registered operations: active ingredient (API) manufacture.
What drugs does Shiratori Pharmaceutical Co., Ltd. make?
2 products are listed under Shiratori Pharmaceutical Co., Ltd. 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.