Prescription drug · NDA
Potassium Chloride NDC 71085-083
Potassium chloride 3 g/3.16g · For solution · Oral · IPG Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71085-083-30 | 71085008330 | 30 POUCH in 1 CARTON (71085-083-30) / 3.16 g in 1 POUCH (71085-083-01)Marketed from Dec 1, 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 — 3 g/3.16g
- Dosage form
- For solution
- Route
- Oral
- Labeler
- IPG Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 208019
- 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 71085-083_dc4ae7ec-789f-4f7e-8a85-c99f3586dabeSPL ID dc4ae7ec-789f-4f7e-8a85-c99f3586dabeSPL set ID 5dad0879-0f97-4c7d-98fa-baaed51cd2d8RxCUI 2728724UNII 660YQ98I10
- 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
N471085008330followed by a unit qualifier and the quantityPackage 71085-0083-30. 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
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Potassium Chloride is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. Potassium Chloride is a potassium salt indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. ( 1 )
Excerpt only. Read the full label for complete information.
Other NDCs under NDA 208019
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 |
|---|---|---|---|---|
| Pokonzapotassium chloride | Potassium chloride 1.125 g/1.185g | Powder, For solutionOral | Carwin Pharmaceutical Associates, LLC | 15370-306 |
| Pokonzapotassium chloride | Potassium chloride .75 g/.79g | Powder, For solutionOral | Carwin Pharmaceutical Associates, LLC | 15370-305 |
| Potassium Chloride | Potassium chloride 1.5 g/1.58g | Powder, For solutionOral | Endo USA, Inc. | 0603-1554 |
| Potassium Chloride | Potassium chloride 1.5 g/1.58g | Powder, For solutionOral | Genus Lifesciences Inc. | 64950-321 |