Register entry

SolarisPharmaCorporation

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Registered sites
0
Active NDC listings
5
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

5

5 active NDC listings: 5 human prescription drug. By marketing category: ANDA 5.

Dosage formNDCs
tablet, film coated5
RouteNDCs
oral5
Labeller name on the listingNDCs
solarispharmacorporation5
Catalogue

Marketed products

5
BrandGeneric nameForm / routeNDC
brivaracetambrivaracetamtablet, film coated, oral73473-904ANDA
brivaracetambrivaracetamtablet, film coated, oral73473-905ANDA
brivaracetambrivaracetamtablet, film coated, oral73473-906ANDA
brivaracetambrivaracetamtablet, film coated, oral73473-907ANDA
brivaracetambrivaracetamtablet, film coated, oral73473-908ANDA
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Other companies listing brivaracetam

Enquiry

Common questions

Is SolarisPharmaCorporation FDA approved?
SolarisPharmaCorporation holds no registered establishment of its own; 5 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does SolarisPharmaCorporation make?
5 products are listed under SolarisPharmaCorporation in the openFDA NDC Directory, most often as tablet, film coated. 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.