Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Japan
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1Finished drug manufacture1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Daito Pharmaceutical Co., Ltd | 326 Yokamachi, Toyama-City, Toyama 939-8221, Japan (JPN) | Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture | 3002806779691240774 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Azelastine Hydrochloride | powder | 60656-1839BULK INGREDIENT |
Neighbours
Registered in the same town
1- Juzen Chemical CorporationToyama-city, JPN
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Enquiry
Common questions
- Is Daito Pharmaceutical Co., Ltd FDA approved?
- Daito 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 Daito Pharmaceutical Co., Ltd's drugs manufactured?
- The FDA register lists Toyama-City. Registered operations: analytical testing, active ingredient (API) manufacture, finished drug manufacture.
- What drugs does Daito Pharmaceutical Co., Ltd make?
- 1 product is listed under Daito 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.