Register entry
Anhui Yinfeng Pharmaceutical 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 |
|---|---|---|---|
| Anhui Yinfeng Pharmaceutical Co., Ltd. | D District, Taihe Economic Development Zone, Fuyang, Anhui 236600, China (CHN) | Active ingredient (API) manufacture | 3010977440421324573 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Menthol | powder | 69155-003BULK INGREDIENT |
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Enquiry
Common questions
- Is Anhui Yinfeng Pharmaceutical Co., Ltd. FDA approved?
- Anhui Yinfeng Pharmaceutical 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 Anhui Yinfeng Pharmaceutical Co., Ltd.'s drugs manufactured?
- The FDA register lists Fuyang. Registered operations: active ingredient (API) manufacture.
- What drugs does Anhui Yinfeng Pharmaceutical Co., Ltd. make?
- 1 product is listed under Anhui Yinfeng 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.