Prescription drug · ANDA
Potassium Chloride NDC 60687-855
Potassium chloride 1.5 g/1.58g · Powder, For solution · Oral · American Health Packaging
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 60687-855-27 | 60687085527 | 30 POUCH in 1 CARTON (60687-855-27) / 1.58 g in 1 POUCH (60687-855-99)Marketed from Mar 28, 2025 | |
| 60687-855-92 | 60687085592 | 100 POUCH in 1 CARTON (60687-855-92) / 1.58 g in 1 POUCH (60687-855-99)Marketed from Mar 28, 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 — 1.5 g/1.58g
- Dosage form
- Powder, For solution
- Route
- Oral
- Labeler
- American Health Packaging
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 211667
- Marketing start
- Listing expires
- Identifiers
- Product ID 60687-855_3d31786f-bf4f-3705-e063-6294a90a25ecSPL ID 3d31786f-bf4f-3705-e063-6294a90a25ecSPL set ID 149770d0-3a2c-4e75-80a3-ec842907920dRxCUI 1867544UNII 660YQ98I10
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
N460687085527followed by a unit qualifier and the quantityPackage 60687-0855-27. 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 211667
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 1.5 g/1.58g | Powder, For solutionOral | Kesin Pharma Corporation | 81033-413 |
| Potassium Chloride | Potassium chloride 1.5 g/1.58g | Powder, For solutionOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-856 |
| Potassium Chloride | Potassium chloride 1.5 g/1.58g | Powder, For solutionOral | Strides Pharma Science Limited | 64380-875 |