Register entry

Zhejiang Haisen 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
EstablishmentAddressRegistered forFEI / DUNS
Zhejiang Haisen Pharmaceutical Co., Ltd.Xiangtan Village, Liushi Street, Dongyang, Zhejiang 322104, China (CHN)Active ingredient (API) manufacture3003967524421317224
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-Sucralfatepowder69984-001BULK INGREDIENT
Neighbours

Registered in the same town

4
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Comparable companies in China

Enquiry

Common questions

Is Zhejiang Haisen Pharmaceutical Co., Ltd. FDA approved?
Zhejiang Haisen 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 Zhejiang Haisen Pharmaceutical Co., Ltd.'s drugs manufactured?
The FDA register lists Dongyang. Registered operations: active ingredient (API) manufacture.
What drugs does Zhejiang Haisen Pharmaceutical Co., Ltd. make?
1 product is listed under Zhejiang Haisen 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.