Register entry
Weifang Shengtai Medicine Co. , Ltd.
Data as of · How to read this entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- China
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Weifang Shengtai Medicine Co., Ltd.Registrant: Weifang Shengtai Medicine Co. , Ltd. | No. 1202 Fangshan Road, Changle County, Weifang, Shandong 262400, China (CHN) | Active ingredient (API) manufacture | 3010165467421578618 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Dextrose Monohydrate | powder | 40087-1001BULK INGREDIENT |
Neighbours
Registered in the same town
3- Shandong AZC Biotechnology Co., Ltd.Weifang, CHN
- Shandong Guobang Pharmaceutical Co., Ltd.Weifang, CHN
- Zhongfu Pharmaceutical Co LtdWeifang, CHN
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Enquiry
Common questions
- Is Weifang Shengtai Medicine Co. , Ltd. FDA approved?
- Weifang Shengtai Medicine Co. , Ltd. holds 1 FDA-registered establishment in China. 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 Weifang Shengtai Medicine Co. , Ltd.'s drugs manufactured?
- The FDA register lists Weifang. Registered operations: active ingredient (API) manufacture.
- What drugs does Weifang Shengtai Medicine Co. , Ltd. make?
- 1 product is listed under Weifang Shengtai Medicine 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.