Prescription drug · ANDA
Potassium Chloride NDC 64380-860
Potassium chloride 600 mg/1 · Tablet, Extended release · Oral · Strides Pharma Science Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 64380-860-06 | 64380086006 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-06)Marketed from Nov 19, 2018 | |
| 64380-860-07 | 64380086007 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-07)Marketed from Nov 27, 2018 | |
| 64380-860-08 | 64380086008 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-08)Marketed from Nov 27, 2018 |
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 — 600 mg/1
- Dosage form
- Tablet, Extended release
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 210733
- 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 64380-860_6c661c91-f05d-4a10-8a6c-1fb0e23b35ecSPL ID 6c661c91-f05d-4a10-8a6c-1fb0e23b35ecSPL set ID 0224e5b3-3c49-4e6e-aa78-1abcc6969246RxCUI 312529, 628953UNII 660YQ98I10UPC 0364380860068, 0364380861065
- 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
N464380086006followed by a unit qualifier and the quantityPackage 64380-0860-06. 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 Extended-release Tablets, USP 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 Extended-release Tablets, USP 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 210733
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 750 mg/1 | Tablet, Extended releaseOral | Direct_Rx | 72189-027 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Strides Pharma Science Limited | 64380-861 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Northwind Health Company, LLC | 51655-706 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 71335-1131 |