Register entry

Ayurax, LLC.

Data as of · How to read this entry

Registered sites
0
Active NDC listings
3
Labeller names
2
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

3

3 active NDC listings: 3 human prescription drug. By marketing category: ANDA 2, NDA AUTHORIZED GENERIC 1.

Dosage formNDCs
ointment1
solution1
tablet1
RouteNDCs
oral2
topical1
Labeller name on the listingNDCs
ayurax, llc2
ayurax, llc.1
Catalogue

Marketed products

3
BrandGeneric nameForm / routeNDC
Amcinonideamcinonideointment, topical73308-407ANDA
FOLIC ACIDfolic acidsolution, oral73308-501NDA AUTHORIZED GENERIC
ULTRAMICROSIZE GRISEOFULVINULTRAMICROSIZE GRISEOFULVINtablet, oral73308-435ANDA
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Other companies listing ultramicrosize griseofulvin

Enquiry

Common questions

Is Ayurax, LLC. FDA approved?
Ayurax, LLC. holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Ayurax, LLC. make?
3 products are listed under Ayurax, LLC. in the openFDA NDC Directory, most often as ointment; solution; tablet. 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.