Prescription drug · ANDA
Potassium Chloride NDC 70010-147
Potassium chloride 600 mg/1 · Capsule, Extended release · Oral · Granules Pharmaceuticals Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70010-147-01 | 70010014701 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-147-01)Marketed from Mar 1, 2021 |
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
- Capsule, Extended release
- Route
- Oral
- Labeler
- Granules Pharmaceuticals Inc
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 214686
- 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 70010-147_495d6938-4058-2799-e063-6294a90adc8fSPL ID 495d6938-4058-2799-e063-6294a90adc8fSPL set ID c1f4832d-4d5c-8c49-e053-2a95a90ac9feRxCUI 312504, 315183UNII 660YQ98I10UPC 0370010148017, 0370010147010
- 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
N470010014701followed by a unit qualifier and the quantityPackage 70010-0147-01. 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
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Potassium chloride extended-release capsules are indicated for the treatment and prophylaxis of hypokalemia in adults and children 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 capsules contain potassium chloride, 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 214686
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 | Capsule, Extended releaseOral | Granules Pharmaceuticals Inc | 70010-148 |
| Potassium Chloride | Potassium chloride 600 mg/1 | Capsule, Extended releaseOral | Granules India Ltd | 62207-914 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Capsule, Extended releaseOral | Granules India Ltd | 62207-915 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Capsule, Extended releaseOral | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8442 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Capsule, Extended releaseOral | A-S Medication Solutions | 50090-7469 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Capsule, Extended releaseOral | BluePoint Laboratories | 68001-619 |
| Potassium Chloride | Potassium chloride 750 mg/1 | Capsule, Extended releaseOral | REMEDYREPACK INC. | 70518-4050 |