Prescription drug · ANDA
Potassium Citrate NDC 70518-4477
Potassium citrate 10 meq/1 · Tablet, Extended release · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4477-0 | 7051844770070518447700 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)Marketed from Sep 12, 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 Citrate
- Generic name (nonproprietary)
- potassium citrate
- Active ingredients
- Potassium citrate — 10 meq/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 214420
- Marketing start
- Listing expires
- Other FDA classes
- Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
- Identifiers
- Product ID 70518-4477_5b39b678-4566-f89c-e063-6294a90acc7fSPL ID 5b39b678-4566-f89c-e063-6294a90acc7f
- Pharmacologic class
- Anti-coagulant; Calculi Dissolution Agent
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
N470518447700followed by a unit qualifier and the quantityPackage 70518-4477-00. 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 70518-4477
- What is NDC 70518-4477?
- 70518-4477 is the product NDC for Potassium Citrate, Potassium citrate 10 meq/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 Citrate.
- What is the active ingredient?
- Potassium citrate.
- 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 Citrate?
- 37 other product NDCs are listed under this name. See all Potassium Citrate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Potassium Citrate 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 Citrate | Potassium citrate 540 mg/1 | Tablet, Extended releaseOral | Rising Pharma Holdings, Inc. | 16571-864 | 16571-0864-01 |
| Potassium Citrate | Potassium citrate 1080 mg/1 | Tablet, Extended releaseOral | Rising Pharma Holdings, Inc. | 16571-865 | 16571-0865-01 |
| Potassium Citrate | Potassium citrate 10 meq/1 | TabletOral | Biocomp Pharma, Inc. | 44523-410 | 44523-0410-01 |
| Potassium Citrate | Potassium citrate 10 meq/1 | Tablet, Extended releaseOral | REMEDYREPACK INC. | 70518-3160 | 70518-3160-00 |
| Potassium Citrate | Potassium citrate 5 meq/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-191 | 72865-0191-01 |
| Potassium Citrate | Potassium citrate 5 meq/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc | 31722-129 | 31722-0129-01 |
| Potassium Citrate | Potassium citrate 10 meq/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc | 31722-130 | 31722-0130-01 |
| Potassium Citrate | Potassium citrate 15 meq/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc | 31722-132 | 31722-0132-01 |
| Potassium Citrate | Potassium citrate 15 meq/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 71335-2897 | 71335-2897-01 |
| Potassium Citrate | Potassium citrate 10 meq/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 72162-2120 | 72162-2120-01 |
Other NDCs under ANDA 214420
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 Citrate | Potassium citrate 5 meq/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc | 31722-129 |
| Potassium Citrate | Potassium citrate 10 meq/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc | 31722-130 |
| Potassium Citrate | Potassium citrate 15 meq/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc | 31722-132 |
| Potassium Citrate | Potassium citrate 15 meq/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 71335-2897 |
| Potassium Citrate | Potassium citrate 10 meq/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 72162-2120 |
| Potassium Citrate | Potassium citrate 15 meq/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 72162-2121 |
| Potassium Citrate | Potassium citrate 5 meq/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | 72162-2122 |
| Potassium Citrate | Potassium citrate 5 meq/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-191 |
| Potassium Citrate | Potassium citrate 10 meq/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-192 |
| Potassium Citrate | Potassium citrate 15 meq/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-193 |