Prescription drug · ANDA
Potassium Chloride for Oral Solution NDC 82983-403
Potassium chloride 1.5 g/1.58g · Powder, For solution · Oral · Ajenat Pharmaceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 82983-403-10 | 82983040310 | 100 POUCH in 1 CARTON (82983-403-10) / 1.58 g in 1 POUCH (82983-403-01)Marketed from Mar 1, 2023 | |
| 82983-403-30 | 82983040330 | 30 POUCH in 1 CARTON (82983-403-30) / 1.58 g in 1 POUCH (82983-403-01)Marketed from Mar 1, 2023 |
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 for Oral Solution
- Generic name (nonproprietary)
- potassium chloride for oral solution
- Active ingredients
- Potassium chloride — 1.5 g/1.58g
- Dosage form
- Powder, For solution
- Route
- Oral
- Labeler
- Ajenat Pharmaceuticals LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 212183
- 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 82983-403_4d98ee0a-c312-4ffd-b004-00157a4661e9SPL ID 4d98ee0a-c312-4ffd-b004-00157a4661e9SPL set ID c62c5704-3667-4d4f-8230-3f7f5ed825b1RxCUI 1867544UNII 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
N482983040310followed by a unit qualifier and the quantityPackage 82983-0403-10. 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 ANDA 212183
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 for Oral Solution | Potassium chloride 1.5 g/1.58g | Powder, For solutionOral | BPI Labs LLC | 54288-125 |
| Potassium Chloride for Oral Solution | Potassium chloride 1.5 g/1.58g | SolutionOral | Marlex Pharmaceuticals Inc | 10135-819 |
| Potassium Chloride for Oral Solution | Potassium chloride 3 g/4.75g | SolutionOral | Marlex Pharmaceuticals Inc | 10135-820 |
| Potassium Chloride for Oral Solution | Potassium chloride 1.5 g/1.58g | Powder, For solutionOral | Marlex Pharmaceuticals, Inc. | 10135-807 |