Register entry

Beach Products, Inc.

Data as of · How to read this entry

Registered sites
0
Active NDC listings
3
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

3

3 active NDC listings: 3 human prescription drug. By marketing category: UNAPPROVED DRUG OTHER 3.

Dosage formNDCs
tablet, coated2
tablet, soluble1
RouteNDCs
oral3
Labeller name on the listingNDCs
beach products, inc.3
Catalogue

Marketed products

3
BrandGeneric nameForm / routeNDC
K Phos NeutralSodium Phosphate, Dibasic, Anhydrous, Potassium Phosphate, Monobasic, and Sodium Phosphate, Monobasic, Monohydratetablet, coated, oral0486-1125UNAPPROVED DRUG OTHER
K Phos OriginalPotassium Phosphate, Monobasictablet, soluble, oral0486-1111UNAPPROVED DRUG OTHER
K-Phos No. 2Potassium Phosphate, Monobasic and Sodium Phosphate, Monobasic, Anhydroustablet, coated, oral0486-1134UNAPPROVED 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.