Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human prescription drug. By marketing category: UNAPPROVED DRUG OTHER 3.
| Dosage form | NDCs |
|---|---|
| tablet, coated | 2 |
| tablet, soluble | 1 |
| Route | NDCs |
|---|---|
| oral | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| beach products, inc. | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| K Phos Neutral | Sodium Phosphate, Dibasic, Anhydrous, Potassium Phosphate, Monobasic, and Sodium Phosphate, Monobasic, Monohydrate | tablet, coated, oral | 0486-1125UNAPPROVED DRUG OTHER |
| K Phos Original | Potassium Phosphate, Monobasic | tablet, soluble, oral | 0486-1111UNAPPROVED DRUG OTHER |
| K-Phos No. 2 | Potassium Phosphate, Monobasic and Sodium Phosphate, Monobasic, Anhydrous | tablet, coated, oral | 0486-1134UNAPPROVED DRUG OTHER |
Enquiry
Common questions
- Is Beach Products, Inc. FDA approved?
- Beach Products, Inc. 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 Beach Products, Inc. make?
- 3 products are listed under Beach Products, Inc. in the openFDA NDC Directory, most often as tablet, coated; tablet, soluble. 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.