Register entry

Nuvaila Limited

Data as of · How to read this entry

Registered sites
0
Active NDC listings
12
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

12

12 active NDC listings: 12 human prescription drug. By marketing category: BLA 11, ANDA 1.

Dosage formNDCs
injection, solution7
injection4
tablet, delayed release1
RouteNDCs
subcutaneous10
intravenous1
oral1
Labeller name on the listingNDCs
nuvaila limited12
Catalogue

Marketed products

12
BrandGeneric nameForm / routeNDC
AMJEVITAadalimumab-attoinjection, subcutaneous84612-399BLA
AMJEVITAadalimumab-attoinjection, subcutaneous84612-479BLA
AMJEVITAadalimumab-attoinjection, subcutaneous84612-481BLA
AMJEVITAadalimumab-attoinjection, subcutaneous84612-482BLA
MesalamineMesalaminetablet, delayed release, oral84612-175ANDA
WEZLANAustekinumab-auubinjection, solution, subcutaneous84612-055BLA
WEZLANAustekinumab-auubinjection, solution, intravenous84612-066BLA
WEZLANAustekinumab-auubinjection, solution, subcutaneous84612-076BLA
WEZLANAustekinumab-auubinjection, solution, subcutaneous84612-089BLA
WEZLANAustekinumab-auubinjection, solution, subcutaneous84612-855BLA
WEZLANAustekinumab-auubinjection, solution, subcutaneous84612-876BLA
WEZLANAustekinumab-auubinjection, solution, subcutaneous84612-889BLA
Enquiry

Common questions

Is Nuvaila Limited FDA approved?
Nuvaila Limited holds no registered establishment of its own; 12 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Nuvaila Limited make?
12 products are listed under Nuvaila Limited in the openFDA NDC Directory, most often as injection, solution; injection; tablet, delayed release. 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.