Prescription drug · NDA
Potassium Chloride NDC 0603-1542
Potassium chloride 20 meq/15mL · Solution · Oral · Endo USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0603-1542-58 | 00603154258 | 473 mL in 1 BOTTLE, PLASTIC (0603-1542-58)Marketed from May 4, 2015 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 20 meq/15mL
- Dosage form
- Solution
- Route
- Oral
- Labeler
- Endo USA, Inc.
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 206814
- Marketing start
- Marketing end
- 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 0603-1542_f57f6d4a-b7d8-407b-8259-19dff55a841dSPL ID f57f6d4a-b7d8-407b-8259-19dff55a841dSPL set ID e5214432-3517-4a90-9412-036752bd1139RxCUI 312515, 314182UNII 660YQ98I10UPC 0306031543586, 0306031542589
- 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
N400603154258followed by a unit qualifier and the quantityPackage 00603-1542-58. 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 are insufficient. 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 are insufficient. ( 1 )
Excerpt only. Read the full label for complete information.
Other NDCs under NDA 206814
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 20 meq/15mL | SolutionOral | Genus Lifesciences | 64950-320 |
| POKONZA potassium chloridepotassium chloride | Potassium chloride 10 meq/15mL | LiquidOral | Carwin Pharmaceutical Associates, LLC | 15370-307 |