Register entry
Kyorin Pharmaceutical Group Facilities Co., Ltd.
Data as of · How to read this entry
- Registered sites
- 1
- Active NDC listings
- 0
- Live patents
- 0
- Countries
- 1
- Base
- Japan
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1Labelling1Packaging1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Kyorin Pharmaceutical Group Facilities Co., Ltd. | 1, Matsubara, Noshiro-shi, Akita 016-0000, Japan (JPN) | Analytical testing, Active ingredient (API) manufacture, Labelling, Packaging | 3003604938717689118 |
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Enquiry
Common questions
- Is Kyorin Pharmaceutical Group Facilities Co., Ltd. FDA approved?
- Kyorin Pharmaceutical Group Facilities 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 Kyorin Pharmaceutical Group Facilities Co., Ltd.'s drugs manufactured?
- The FDA register lists Noshiro-shi. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, packaging.
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.