Prescription drug · NDA
Potassium Chloride NDC 0603-1554
Potassium chloride 1.5 g/1.58g · Powder, For solution · Oral · Endo USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0603-1554-04 | 00603155404 | 100 POUCH in 1 CARTON (0603-1554-04) / 1.58 g in 1 POUCH (0603-1554-10)Marketed from Sep 18, 2015 | |
| 0603-1554-16 | 00603155416 | 30 POUCH in 1 CARTON (0603-1554-16) / 1.58 g in 1 POUCH (0603-1554-10)Marketed from Sep 18, 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 — 1.5 g/1.58g
- Dosage form
- Powder, For solution
- Route
- Oral
- Labeler
- Endo USA, Inc.
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 208019
- Marketing start
- Listing expires
- Identifiers
- Product ID 0603-1554_05260a26-2484-4fd1-9ca1-8445f239923eSPL ID 05260a26-2484-4fd1-9ca1-8445f239923eSPL set ID a64d7151-09a6-474c-83fc-36c7cf582d32RxCUI 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
N400603155404followed by a unit qualifier and the quantityPackage 00603-1554-04. 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 | Genus Lifesciences Inc. | 64950-321 |
| Potassium Chloride | Potassium chloride 3 g/3.16g | For solutionOral | IPG Pharmaceuticals, Inc. | 71085-083 |