Register entry

Pharmakina S.A.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
2
Live patents
0
Countries
1
Base
COG
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
PHARMAKINA S.A.Registrant: Pharmakina S.A.Km 4, Route de Gomma, Bukavu, South Kivu Province 1240, Congo - Brazzaville (COG)Active ingredient (API) manufacture3015820051850503128
Catalogue

Drug listings by form and route

2

2 active NDC listings: 2 bulk ingredient. By marketing category: BULK INGREDIENT 2.

Dosage formNDCs
powder2
RouteNDCs
Labeller name on the listingNDCs
pharmakina s.a.2
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
-QUININE HYDROCHLORIDEpowder67729-000BULK INGREDIENT
-QUININE SULFATEpowder67729-001BULK INGREDIENT
Enquiry

Common questions

Is Pharmakina S.A. FDA approved?
Pharmakina S.A. holds 1 FDA-registered establishment in COG. 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 Pharmakina S.A.'s drugs manufactured?
The FDA register lists Bukavu. Registered operations: active ingredient (API) manufacture.
What drugs does Pharmakina S.A. make?
2 products are listed under Pharmakina S.A. 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.