Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Taiwan
Authorisation
Registered operations
Analytical testing1Labelling1Finished drug manufacture1Packaging1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Orient Pharma Co., Ltd. QC LABORATORYRegistrant: Orient Pharma Co., Ltd. | Rm. A342, A334, A335, A356, A338 and A339, 3F, No. 16, Kehu 1st Rd., Huwei Township, Yunlin County, 632007, Taiwan (TWN) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 3009057557658875409 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Ezetimibe | Ezetimibe | tablet, oral | 76333-170ANDA |
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Enquiry
Common questions
- Is Orient Pharma Co., Ltd. FDA approved?
- Orient Pharma Co., Ltd. holds 1 FDA-registered establishment in Taiwan. 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 Orient Pharma Co., Ltd.'s drugs manufactured?
- The FDA register lists Yunlin County. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.
- What drugs does Orient Pharma Co., Ltd. make?
- 1 product is listed under Orient Pharma Co., Ltd. in the openFDA NDC Directory, most often as tablet. 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.