Register entry

Guilin 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
Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Guilin Pharmaceutical Co., Ltd.Registrant: Guilin Pharmaceutical Co LtdNo.43 Qilidian Road, Qixing District, Guilin, Guangxi 541004, China (CHN)Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging3002807125654265578
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-Bumetanidepowder57755-0004BULK INGREDIENT
Neighbours

Registered in the same town

1
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Comparable companies in China

Enquiry

Common questions

Is Guilin Pharmaceutical Co Ltd FDA approved?
Guilin 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 Guilin Pharmaceutical Co Ltd's drugs manufactured?
The FDA register lists Guilin. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
What drugs does Guilin Pharmaceutical Co Ltd make?
1 product is listed under Guilin 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.