Register entry

Novartis Pharma Schweizerhalle AG

Data as of · How to read this entry

Registered sites
0
Active NDC listings
6
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

6

6 active NDC listings: 6 bulk ingredient. By marketing category: BULK INGREDIENT 6.

Dosage formNDCs
powder5
liquid1
RouteNDCs
Labeller name on the listingNDCs
novartis pharma schweizerhalle ag6
Catalogue

Marketed products

6
BrandGeneric nameForm / routeNDC
-INCLISIRANliquid44139-0101BULK INGREDIENT
-IPTACOPANpowder44139-0100BULK INGREDIENT
-TRAMETINIB DIMETHYL SULFOXIDEpowder44139-0102BULK INGREDIENT
-asciminib hydrochloridepowder44139-0104BULK INGREDIENT
-eltrombopag olaminepowder44139-0105BULK INGREDIENT
-fingolimod hydrochloridepowder44139-0103BULK INGREDIENT
Enquiry

Common questions

Is Novartis Pharma Schweizerhalle AG FDA approved?
Novartis Pharma Schweizerhalle AG holds no registered establishment of its own; 6 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Novartis Pharma Schweizerhalle AG make?
6 products are listed under Novartis Pharma Schweizerhalle AG in the openFDA NDC Directory, most often as powder; liquid. 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.