Register entry
- Registered sites
- 1
- Active NDC listings
- 2
- Live patents
- 0
- Countries
- 1
- Base
- COG
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| PHARMAKINA S.A.Registrant: Pharmakina S.A. | Km 4, Route de Gomma, Bukavu, South Kivu Province 1240, Congo - Brazzaville (COG) | Active ingredient (API) manufacture | 3015820051850503128 |
Catalogue
Drug listings by form and route
22 active NDC listings: 2 bulk ingredient. By marketing category: BULK INGREDIENT 2.
| Dosage form | NDCs |
|---|---|
| powder | 2 |
| Route | NDCs |
|---|
| Labeller name on the listing | NDCs |
|---|---|
| pharmakina s.a. | 2 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | QUININE HYDROCHLORIDE | powder | 67729-000BULK INGREDIENT |
| - | QUININE SULFATE | powder | 67729-001BULK 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.