Register entry

Shenzhen Oriental Pharmaceutical Co. Ltd

Data as of · How to read this entry

Registered sites
1
Active NDC listings
3
Labeller names
3
Live patents
0
Countries
1
Base
China
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Shenzhen Oriental Pharmaceutical Co. LtdNo. 43 Dakeng Rd., Tongle Village, Shenzhen 518116, China (CHN)Active ingredient (API) manufacture3003677845529234171
Catalogue

Drug listings by form and route

3

3 active NDC listings: 3 bulk ingredient. By marketing category: BULK INGREDIENT 3.

Dosage formNDCs
powder3
RouteNDCs
Labeller name on the listingNDCs
shenzhen oriental pharmaceutical co. ltd1
shenzhen oriental pharmaceutical co. ltd.1
shenzhen oriental pharmaceutical co., ltd.1
Catalogue

Marketed products

3
BrandGeneric nameForm / routeNDC
-Doxylamine Succinatepowder64431-0003BULK INGREDIENT
-Phenylephrine Bitartratepowder64431-0004BULK INGREDIENT
-Phenylephrine Hydrochloridepowder64431-0001BULK INGREDIENT
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Comparable companies in China

Enquiry

Common questions

Is Shenzhen Oriental Pharmaceutical Co. Ltd FDA approved?
Shenzhen Oriental 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 Shenzhen Oriental Pharmaceutical Co. Ltd's drugs manufactured?
The FDA register lists Tongle Village. Registered operations: active ingredient (API) manufacture.
What drugs does Shenzhen Oriental Pharmaceutical Co. Ltd make?
3 products are listed under Shenzhen Oriental 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.