Uses
1 INDICATIONS AND USAGE Renal Tubular Acidosis (RTA) with Calcium Stones Potassium Citrate is indicated for the management of renal tubular acidosis.
Source: US FDA prescribing information
Molecule
Potassium citrate is an anti-coagulant indicated for the management of renal tubular acidosis, among other approved uses. It is available as extended-release tablets and tablets for oral use. MedsAcross supplies Potassium citrate for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
From the regulator-approved product information. Each section names its source.
1 INDICATIONS AND USAGE Renal Tubular Acidosis (RTA) with Calcium Stones Potassium Citrate is indicated for the management of renal tubular acidosis.
Source: US FDA prescribing information
When Potassium Citrate is given orally, the metabolism of absorbed citrate produces an alkaline load. The induced alkaline load in turn increases urinary pH and raises urinary citrate by augmenting citrate clearance without measurably altering ultrafilterable serum citrate. Thus, Potassium Citrate therapy appears to increase urinary citrate principally by modifying the renal handling of citrate, rather than by increasing the filtered load of citrate. The increased filtered load of citrate may play some role, however, as in small comparisons of oral citrate and oral bicarbonate, citrate had a greater effect on urinary citrate. In addition to raising urinary pH and citrate, Potassium Citrate increases urinary potassium by approximately the amount contained in the medication. In some patients, Potassium Citrate causes a transient reduction in urinary calcium.
Source: US FDA prescribing information
2 DOSAGE AND ADMINISTRATION Dosing Instructions Treatment with extended release Potassium Citrate should be added to a regimen that limits salt intake (avoidance of foods with high salt content and of added salt at the table) and encourages high fluid intake (urine volume should be at least two liters per day). The objective of treatment with Potassium Citrate is to provide Potassium Citrate in sufficient dosage to restore normal urinary citrate (greater than 320 mg/day and as close to the normal mean of 640 mg/day as possible), and to increase urinary pH to a level of 6.0 or 7.0. Monitor serum electrolytes (sodium, potassium, chloride and carbon dioxide), serum creatinine and complete blood counts every four months and more frequently in patients with cardiac disease, renal disease or acidosis. Perform electrocardiograms periodically.
Source: US FDA prescribing information
Potassium Citrate is contraindicated: In patients with hyperkalemia (or who have conditions pre-disposing them to hyperkalemia), as a further rise in serum potassium concentration may produce cardiac arrest. Such conditions include: chronic renal failure, uncontrolled diabetes mellitus, acute dehydration, strenuous physical exercise in unconditioned individuals, adrenal insufficiency, extensive tissue breakdown or the administration of a potassium-sparing agent (such as triamterene, spironolactone or amiloride).
Source: US FDA prescribing information
5 WARNINGS AND PRECAUTIONS Hyperkalemia In patients with impaired mechanisms for excreting potassium, Potassium Citrate administration can produce hyperkalemia and cardiac arrest. Potentially fatal hyperkale- mia can develop rapidly and be asymptomatic. The use of Potassium Citrate in patients with chronic renal failure, or any other condition which impairs potassium excretion such as severe myocardial damage or heart failure, should be avoided. Closely monitor for signs of hyperkalemia with periodic blood tests and ECGs.
Source: US FDA prescribing information
Postmarketing Experience Some patients may develop minor gastrointestinal complaints during Potassium Citrate therapy, such as abdominal discomfort, vomiting, diarrhea, loose bowel movements or nausea. These symptoms are due to the irritation of the gastrointestinal tract, and may be alleviated by taking the dose with meals or snacks, or by reducing the dosage. Patients may find intact matrices in their feces. Some patients may develop minor gastrointestinal complaints such as abdominal discomfort, vomiting, diarrhea, loose bowel movements or nausea. These may be alleviated by taking the dose with meals or snacks or by reducing the dosage
Source: US FDA prescribing information
7 DRUG INTERACTIONS Potential Effects of Potassium Citrate on Other Drugs Potassium-sparing Diuretics: Concomitant administration of Potassium Citrate and a potassium-sparing diuretic (such as triamterene, spironolactone or amiloride) should be avoided since the simultaneous administration of these agents can produce severe hyperkalemia.
Source: US FDA prescribing information
Store in a tight container.
Source: US FDA prescribing information
For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
10 presentations of Potassium citrate, sorted by availability.
| Medicine | Manufacturer | Register | Availability |
|---|---|---|---|
| Potassium citrate 10 mEq extended-release tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 15 mEq extended-release tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 5 mEq extended-release tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 10 mEq tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 15 mEq tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 5 mEq tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 1080 mg extended-release tabletOralGeneric name | — | US FDA | Available on request |
| Potassium citrate 540 mg extended-release tabletOralGeneric name | — | US FDA | Available on request |
| Urocit-k 10 mEq extended-release tabletOral | Mission Pharmacal | US FDA | Available on request |
| Urocit-k 15 mEq extended-release tabletOral | Mission Pharmacal | US FDA | Available on request |
1 brand names across 1 markets.
United States
Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.
| Register | Status | Source |
|---|---|---|
| US FDA | First approved 30 August 1985 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Conditions linked to Potassium citrate in public data. This is not a list of approved uses, see the clinical information.
Yes, on request. MedsAcross lists 10 presentations of Potassium citrate and sources them for licensed hospitals, importers and physicians against valid import documents.
The catalogue lists 1 brand names for Potassium citrate, including Urocit-k.
Yes. The US FDA first approved Potassium citrate on 30 August 1985, according to Drugs@FDA.
No listed presentation of Potassium citrate is recorded as needing a cold chain. Storage conditions are shown on each presentation page.
Potassium citrate is classified under ATC code A12BA02 (Potassium citrate).
Tell us the strength, quantity and destination country. Our team replies with availability, lead time and the import documents needed.