Prescription drug · ANDA
Potassium chloride NDC 72789-504
Potassium chloride 1500 mg/1 · Tablet, Film coated, Extended release · Oral · PD-Rx Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72789-504-82 | 72789050482 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-504-82)Marketed from May 12, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Potassium chloride
- Generic name (nonproprietary)
- potassium chloride
- Active ingredients
- Potassium chloride — 1500 mg/1
- Dosage form
- Tablet, Film coated, Extended release
- Route
- Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 215725
- Marketing start
- Listing expires
- Other FDA classes
- Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
- Identifiers
- Product ID 72789-504_5b9e06b0-08a7-7fcc-e063-6294a90af5f6SPL ID 5b9e06b0-08a7-7fcc-e063-6294a90af5f6
- Pharmacologic class
- Osmotic Laxative; Potassium Salt
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N472789050482followed by a unit qualifier and the quantityPackage 72789-0504-82. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
The FDA listing for this product does not reference a label (SPL) set.
Other NDCs under ANDA 215725
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Potassium chloride | Potassium chloride 750 mg/1 | Tablet, Film coated, Extended releaseOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-960 |
| Potassium chloride | Potassium chloride 1125 mg/1 | Tablet, Film coated, Extended releaseOral | Advagen Pharma Ltd | 72888-201 |
| Potassium chloride | Potassium chloride 750 mg/1 | Tablet, Film coated, Extended releaseOral | PD-Rx Pharmaceuticals, Inc. | 72789-503 |
| Potassium chloride | Potassium chloride 750 mg/1 | Tablet, Film coated, Extended releaseOral | Advagen Pharma Ltd | 72888-075 |
| Potassium chloride | Potassium chloride 1500 mg/1 | Tablet, Film coated, Extended releaseOral | Advagen Pharma Ltd | 72888-076 |
| Potassium chloride | Potassium chloride 750 mg/1 | Tablet, Film coated, Extended releaseOral | A-S Medication Solutions | 50090-7748 |
| Potassium chloride | Potassium chloride 750 mg/1 | Tablet, Film coated, Extended releaseOral | A-S Medication Solutions | 50090-7749 |