Is Meiji Seika Pharma Co., Ltd. FDA approved?

Meiji Seika Pharma Co., Ltd. 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 Meiji Seika Pharma Co., Ltd.'s drugs manufactured?

The FDA register lists Kitakami; Motosu-gun; Odawara. Registered operations: analytical testing, active ingredient (API) manufacture, finished drug manufacture, packaging.

What drugs does Meiji Seika Pharma Co., Ltd. make?

1 product is listed under Meiji Seika Pharma 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.

Meiji Seika Pharma Co., Ltd.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 3
Active NDC listings: 1
Live patents: 0
Countries: 1
Base: Japan

Authorisation

Registered operations

Analytical testing3Active ingredient (API) manufacture2Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Meiji Seika Pharma Co., Ltd.	3-3, Kitakogyodanchi, Kitakami, Iwate 024-0002, Japan (JPN)	Analytical testing, Active ingredient (API) manufacture	3002902776695400580
Meiji Seika Pharma Co., Ltd.	2890, Kitagata, Kitagatacho, Motosu-gun, Gifu 501-0431, Japan (JPN)	Analytical testing, Active ingredient (API) manufacture	3008927877695400606
Meiji Seika Pharmatech Co., Ltd.Registrant: Meiji Seika Pharma Co., Ltd.	1056, Kamonomiya, Odawara, Kanagawa 250-0874, Japan (JPN)	Analytical testing, Finished drug manufacture, Packaging	3015407855739489196

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Doxorubicin	powder	12543-3209BULK INGREDIENT

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Enquiry

Common questions

Is Meiji Seika Pharma Co., Ltd. FDA approved?: Meiji Seika Pharma Co., Ltd. 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 Meiji Seika Pharma Co., Ltd.'s drugs manufactured?: The FDA register lists Kitakami; Motosu-gun; Odawara. Registered operations: analytical testing, active ingredient (API) manufacture, finished drug manufacture, packaging.
What drugs does Meiji Seika Pharma Co., Ltd. make?: 1 product is listed under Meiji Seika Pharma 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.