Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human prescription drug. By marketing category: ANDA 2, NDA AUTHORIZED GENERIC 1.
| Dosage form | NDCs |
|---|---|
| ointment | 1 |
| solution | 1 |
| tablet | 1 |
| Route | NDCs |
|---|---|
| oral | 2 |
| topical | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| ayurax, llc | 2 |
| ayurax, llc. | 1 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Amcinonide | amcinonide | ointment, topical | 73308-407ANDA |
| FOLIC ACID | folic acid | solution, oral | 73308-501NDA AUTHORIZED GENERIC |
| ULTRAMICROSIZE GRISEOFULVIN | ULTRAMICROSIZE GRISEOFULVIN | tablet, oral | 73308-435ANDA |
Compare
Other companies listing ultramicrosize griseofulvin
- Chartwell RX, LLC.0 sites · 580 NDC
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.