Prescription drug · ANDA
Potassium Chloride Extended Release (Potassium chloride) NDC 70518-4520
Potassium chloride 750 mg/1 · Tablet, Extended release · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4520-0 | 70518452000 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4520-0)Marketed from Nov 21, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 Extended Release
- Generic name (nonproprietary)
- potassium chloride
- Active ingredients
- Potassium chloride — 750 mg/1
- Dosage form
- Tablet, Extended release
- Route
- Oral
- Labeler
- REMEDYREPACK INC.NDC labeler code 70518
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 211797
- 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 70518-4520_5b8916b8-ebae-dc8c-e063-6394a90a79e5SPL ID 5b8916b8-ebae-dc8c-e063-6394a90a79e5
- 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
N470518452000followed by a unit qualifier and the quantityPackage 70518-4520-00. 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.
About NDC 70518-4520
- What is NDC 70518-4520?
- 70518-4520 is the product NDC for Potassium Chloride Extended Release, Potassium chloride 750 mg/1 tablet, extended release, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Potassium Chloride Extended Release (Potassium chloride).
- What is the active ingredient?
- Potassium chloride.
- Who is the labeler?
- REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Potassium Chloride Extended Release?
- 46 other product NDCs are listed under this name. See all Potassium Chloride Extended Release NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Potassium Chloride Extended Release products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Potassium Chloride Extended-Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Major Pharmaceuticals | 0904-7547 | 00904-7547-61 |
| Potassium Chloride Extended-release | Potassium chloride 1500 mg/1 | Tablet, Extended releaseOral | REMEDYREPACK INC. | 70518-4383 | 70518-4383-0070518-4383-0170518-4383-02 |
| Potassium Chloride Extended Releasepotassium chloride | Potassium chloride 600 mg/1 | Tablet, Extended releaseOral | Rising Pharma Holdings, Inc. | 16571-842 | 16571-0842-0116571-0842-1016571-0842-50 |
| Potassium Chloride Extended Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Rising Pharma Holdings, Inc. | 16571-843 | 16571-0843-0116571-0843-1016571-0843-50 |
| Potassium Chloride Extended-release | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | REMEDYREPACK INC. | 70518-4095 | 70518-4095-0270518-4095-03 |
| Potassium Chloride Extended-Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Upsher-Smith Laboratories, LLC | 24979-231 | 24979-0231-0124979-0231-0224979-0231-03 |
| Potassium Chloride Extended-Releasepotassium chloride | Potassium chloride 1500 mg/1 | Tablet, Extended releaseOral | Upsher-Smith Laboratories, LLC | 24979-232 | 24979-0232-0124979-0232-02 |
| Potassium Chloride Extended-Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | A-S Medication Solutions | 50090-6639 | 50090-6639-0050090-6639-0150090-6639-02+1 more |
| Potassium Chloride Extended-Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | A-S Medication Solutions | 50090-6640 | 50090-6640-00 |
| Potassium Chloride Extended-Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 71335-2447 | 71335-2447-0171335-2447-0271335-2447-03+4 more |
Other NDCs under ANDA 211797
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 Extended Releasepotassium chloride | Potassium chloride 600 mg/1 | Tablet, Extended releaseOral | Granules Pharmaceuticals Inc. | 70010-021 |
| Potassium Chloride Extended Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Granules Pharmaceuticals Inc. | 70010-022 |
| Potassium Chloride Extended Releasepotassium chloride | Potassium chloride 750 mg/1 | Tablet, Extended releaseOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-932 |