Register entry

ChemPacific Corporation

Data as of · How to read this entry

Registered sites
2
Active NDC listings
1
Live patents
0
Countries
2
Base
United States
Authorisation

Registered operations

Active ingredient (API) manufacture2
Sites

Registered establishments

2
EstablishmentAddressRegistered forFEI / DUNS
Zhejiang ChemPacific CorporationRegistrant: ChemPacific CorporationEast Blvd, Jiaxiang Port, Zhapu, Jiaxing, Zhejiang 314201, China (CHN)Active ingredient (API) manufacture3005632618529129333
ChemPacific Corporation6200 Seaforth Street, Baltimore, Maryland (MD) 21224, United States (USA)Active ingredient (API) manufacture3003299802947763298
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-Norepinephrine Bitartratepowder66300-001BULK INGREDIENT
Neighbours

Registered in the same town

9
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Comparable companies in United States

Enquiry

Common questions

Is ChemPacific Corporation FDA approved?
ChemPacific Corporation holds 2 FDA-registered establishments across 2 countries. 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 ChemPacific Corporation's drugs manufactured?
At registered sites in China, the United States. The FDA register lists Jiaxing; Baltimore, MD. Registered operations: active ingredient (API) manufacture.
What drugs does ChemPacific Corporation make?
1 product is listed under ChemPacific Corporation 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.