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 prescription drug. By marketing category: UNAPPROVED DRUG OTHER 2.
| Dosage form | NDCs |
|---|---|
| cream | 1 |
| gel | 1 |
| Route | NDCs |
|---|---|
| dental | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| cypress pharmaceutical, inc. | 2 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| SF | 1.1% Sodium Fluoride | gel, dental | 60258-151UNAPPROVED DRUG OTHER |
| SF 5000 Plus | 1.1% Sodium Fluoride Prescription Dental Cream | cream, dental | 60258-150UNAPPROVED DRUG OTHER |
Compare
Other companies listing 1.1% sodium fluoride
- Benco Dental0 sites · 33 NDC
Enquiry
Common questions
- Is Cypress Pharmaceutical, Inc. FDA approved?
- Cypress Pharmaceutical, 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 Cypress Pharmaceutical, Inc. make?
- 2 products are listed under Cypress Pharmaceutical, Inc. in the openFDA NDC Directory, most often as cream; gel. 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.