Prescription drug · ANDA
Potassium Chloride NDC 71656-022
Potassium chloride 3 g/15mL · Solution · Oral · Saptalis Pharmaceuticals, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71656-022-01 | 71656002201 | 10 TRAY in 1 CASE (71656-022-01) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-022-15)Marketed from Oct 5, 2023 | |
| 71656-022-16 | 71656002216 | 473 mL in 1 BOTTLE (71656-022-16)Marketed from Oct 5, 2023 | |
| 71656-022-50 | 71656002250 | 5 TRAY in 1 CASE (71656-022-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-022-15)Marketed from Oct 5, 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
- Generic name (nonproprietary)
- potassium chloride
- Active ingredients
- Potassium chloride — 3 g/15mL
- Dosage form
- Solution
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 211648
- 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 71656-022_5c17860b-20f1-2b92-e063-6294a90af2a4SPL ID 5c17860b-20f1-2b92-e063-6294a90af2a4
- 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
N471656002201followed by a unit qualifier and the quantityPackage 71656-0022-01. 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
The FDA listing for this product does not reference a label (SPL) set.
Other NDCs under ANDA 211648
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 Chloridepotassium chloride oral | Potassium chloride 1.5 g/15mL | SolutionOral | Cardinal Health 107, LLC | 55154-8026 |
| Potassium Chloridepotassium chloride oral | Potassium chloride 1.5 g/15mL | SolutionOral | Saptalis Pharmaceuticals, LLC | 71656-021 |
| Potassium Chloridepotassium chloride oral | Potassium chloride 1.5 g/15mL | SolutionOral | American Health Packaging | 60687-884 |
| Potassium Chloride | Potassium chloride 1.5 g/15mL | SolutionOral | American Health Packaging | 60687-628 |
| Potassium Chloridepotassium chloride oral | Potassium chloride 1.5 g/15mL | SolutionOral | ATLANTIC BIOLOGICALS CORP. | 17856-0048 |
| Potassium Chloride | Potassium chloride 3 g/30mL | SolutionOral | Kesin Pharma Corporation | 81033-240 |
| Potassium Chloride | Potassium chloride 1.5 g/15mL | SolutionOral | Kesin Pharma Corporation | 81033-220 |