Register entry
- Registered sites
- 0
- Active NDC listings
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
22 active NDC listings: 2 human otc drug. By marketing category: ANDA 2.
| Dosage form | NDCs |
|---|---|
| aerosol, foam | 2 |
| Route | NDCs |
|---|---|
| topical | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| spazi inc. | 2 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Minoxidil (For Men) | Minoxidil | aerosol, foam, topical | 82376-6006ANDA |
| Minoxidil (For Women) | Minoxidil | aerosol, foam, topical | 82376-6007ANDA |
Compare
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Enquiry
Common questions
- Is SPAZI INC. FDA approved?
- SPAZI INC. holds no registered establishment of its own; 2 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does SPAZI INC. make?
- 2 products are listed under SPAZI INC. in the openFDA NDC Directory, most often as aerosol, foam. 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.