Drug company (FDA labeler)
Affordable Pharmaceuticals, LLC
NDC labeler code: 10572
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- Sodium sulfate, potassium sulfate, magnesium sulfateSuprep Bowel Prep, Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep Kit · 2 products
- Polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloridePEG 3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride, Trilyte, Peg-3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride · 1 product
- Polyethylene glycol 3350, sodium sulfate anhydrous, sodium bicarbonate, sodium chloride, potassium chloridePeg-3350 and Electrolytes, Golytely, PEG 3350 and Electrolytes · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| August 5, 2010 | NDA022372 | Sodium sulfate, potassium sulfate, magnesium sulfate SUPREP BOWEL PREP KIT | Azurity |
| April 22, 1991 | NDA019797 | Polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride NULYTELY, NULYTELY-FLAVORED | Azurity |
| July 13, 1984 | NDA019011 | Polyethylene glycol 3350, sodium sulfate anhydrous, sodium bicarbonate, sodium chloride, potassium chloride GOLYTELY | Azurity |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
- All drug companiesA to Z
- All prescription drugs A to ZSearch by generic, brand or Spanish name
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026