Register entry
Kyongbo Pharmaceutical Co., Ltd.
Data as of · How to read this entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- South Korea
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Kyongbo Pharmaceutical Co., Ltd. | 174 Sirok-Ro, Asan, Chungcheongnam-do 315-01, Korea, South (KOR) | Analytical testing, Active ingredient (API) manufacture | 3003773799687781963 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | LENALIDOMIDE | powder | 51065-009BULK INGREDIENT |
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Enquiry
Common questions
- Is Kyongbo Pharmaceutical Co., Ltd. FDA approved?
- Kyongbo Pharmaceutical Co., Ltd. holds 1 FDA-registered establishment in South Korea. 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 Kyongbo Pharmaceutical Co., Ltd.'s drugs manufactured?
- The FDA register lists Chungcheongnam-do 315-01. Registered operations: analytical testing, active ingredient (API) manufacture.
- What drugs does Kyongbo Pharmaceutical Co., Ltd. make?
- 1 product is listed under Kyongbo 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.