Prescription drug · ANDA
Potassium Chloride for Oral Solution NDC 70069-823
potassium chloride · Potassium chloride 1.5 g/1.58g · For solution · Oral · Somerset Therapeutics, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70069-823-01 | 70069082301 | 1.58 g in 1 POUCH (70069-823-01)Marketed from Apr 10, 2025 | |
| 70069-823-10 | 70069082310 | 100 POUCH in 1 CARTON (70069-823-10) / 1.58 g in 1 POUCHMarketed from Apr 10, 2025 | |
| 70069-823-30 | 70069082330 | 30 POUCH in 1 CARTON (70069-823-30) / 1.58 g in 1 POUCHMarketed from Apr 10, 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 for Oral Solution
- Generic name (nonproprietary)
- potassium chloride
- Active ingredients
- Potassium chloride — 1.5 g/1.58g
- Dosage form
- For solution
- Route
- Oral
- Labeler
- Somerset Therapeutics, LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213467
- Marketing start
- Listing expires
- Identifiers
- Product ID 70069-823_32809cac-68f8-94d5-e063-6394a90a9395SPL ID 32809cac-68f8-94d5-e063-6394a90a9395SPL set ID 32809eae-1c3f-96fc-e063-6394a90aeaadRxCUI 1867544UNII 660YQ98I10UPC 0370069823019, 0370069823101, 0370069823309
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
N470069082301followed by a unit qualifier and the quantityPackage 70069-0823-01. 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 for oral solution 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 213467
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 Solutionpotassium chloride | Potassium chloride 1.5 g/1.58g | For solutionOral | Granules Pharmaceuticals Inc. | 70010-071 |