Prescription drug · ANDA
Potassium Chloride for Oral Solution NDC 70010-071
potassium chloride · Potassium chloride 1.5 g/1.58g · For solution · Oral · Granules Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70010-071-41 | 70010007141 | 1.58 g in 1 POUCH (70010-071-41)Marketed from Sep 1, 2023 | |
| 70010-071-42 | 70010007142 | 30 POUCH in 1 CARTON (70010-071-42) / 1.58 g in 1 POUCHMarketed from Sep 1, 2023 | |
| 70010-071-43 | 70010007143 | 100 POUCH in 1 CARTON (70010-071-43) / 1.58 g in 1 POUCHMarketed from Sep 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
- Active ingredients
- Potassium chloride — 1.5 g/1.58g
- Dosage form
- For solution
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213467
- Marketing start
- Listing expires
- Identifiers
- Product ID 70010-071_44f3f63d-4523-91e4-e063-6394a90a6d1bSPL ID 44f3f63d-4523-91e4-e063-6394a90a6d1bSPL set ID 727be945-df2a-4fbf-ade4-f242e2647976RxCUI 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
N470010007141followed by a unit qualifier and the quantityPackage 70010-0071-41. 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.
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 | Somerset Therapeutics, LLC | 70069-823 |