Potassium
Potassium is an essential mineral available in several forms and formulations used to treat or prevent low potassium levels (hypokalemia) and, in citrate form, to manage certain kidney stone conditions.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 272 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
📖 Potassium: Patient Information Guide
A plain-language walkthrough of Potassium — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
Potassium is available in multiple forms and formulations, each with specific approved uses:
- Potassium chloride oral tablets, capsules, liquids, and powders (including POKONZA): treat and prevent hypokalemia (low blood potassium) with or without metabolic alkalosis, when dietary changes or diuretic dose reduction are not enough
- Potassium chloride extended-release oral tablets and capsules: reserved for patients who cannot tolerate or comply with liquid or effervescent potassium — used to treat hypokalemia in digitalis intoxication, hypokalemic familial periodic paralysis, and to prevent hypokalemia in high-risk patients (such as those with significant cardiac arrhythmias, liver disease with ascites, or potassium-losing kidney conditions)
- Potassium chloride intravenous injection: treats potassium deficiency when oral replacement is not possible; specifically intended for fluid-restricted patients who need potassium supplementation without large fluid volumes
- Potassium citrate extended-release tablets (including Urocit-K): manage renal tubular acidosis (RTA) with calcium kidney stones; hypocitraturic calcium oxalate nephrolithiasis (calcium oxalate stones caused by low urinary citrate); and uric acid kidney stones with or without calcium stones
⚙️How it works▾
Potassium chloride works by directly replenishing potassium, an essential mineral the body needs for normal nerve signaling, muscle contractions (including the heart), and fluid balance. When blood potassium drops too low, muscles and the heart can malfunction — replacing it restores normal function.
Potassium citrate works differently. When absorbed, the citrate portion is metabolized into an alkaline compound that raises the pH of urine and increases urinary citrate levels. Citrate binds to calcium in the urine, reducing the amount of free calcium available to form stones. It also makes uric acid more soluble so it won't crystallize. Together, these changes make the urine less likely to produce kidney stones.
💊How it's taken▾
How you take potassium depends entirely on which product and form is prescribed. General principles:
- Oral liquids and powders: always dilute in water or another liquid before drinking — never take undiluted
- Extended-release tablets and capsules: take with meals and a full glass of water; swallow whole unless your label says otherwise
- Potassium citrate tablets: typically taken multiple times per day with meals or within 30 minutes of eating
- IV potassium chloride: given only in a clinical setting through a slow, controlled infusion — never as a rapid injection
Your prescriber will monitor your blood potassium levels and adjust your dose. Do not change your dose on your own, and follow your prescription label exactly.
🤒Side effects — in detail▾
The most common side effects involve the stomach and gut:
- Nausea or vomiting
- Stomach pain or discomfort
- Gastrointestinal irritation
- With IV use: pain, burning, redness, swelling, or inflammation at the infusion site
- Chest pain (IV use)
- Rash or allergic reaction (including swelling)
Serious reactions — including dangerous heart rhythms, cardiac arrest, severe GI bleeding, tissue damage from IV leakage, and low sodium levels — require immediate medical attention and are most likely in high-risk patients or with IV use.
⚠️Warnings & precautions▾
- Hyperkalemia (too much potassium in the blood) is the most dangerous risk. It can cause life-threatening heart arrhythmias and cardiac arrest — sometimes with no warning symptoms. People with kidney disease, heart failure, adrenal insufficiency, or those on potassium-sparing medications are at highest risk. Regular blood tests and heart monitoring are essential.
- GI lesions: extended-release solid forms (tablets and capsules) can cause ulcers and bleeding in the stomach or intestines. Stop the medication and seek care immediately if you have severe stomach pain, vomiting, or signs of bleeding.
- IV-specific risks: too-rapid infusion can cause fatal arrhythmias. If IV solution leaks outside the vein (extravasation), it can cause serious tissue, nerve, and vascular damage — sometimes requiring surgery or amputation. Concentrated potassium IV must only be given through a central line with continuous heart monitoring.
- Hyponatremia (low sodium): IV potassium chloride can cause low blood sodium, which can lead to brain swelling, seizures, and serious neurological harm, especially in children, elderly patients, and postoperative patients.
🔀What it interacts with▾
Several medications can dangerously raise potassium levels or worsen side effects when combined with potassium products:
- Potassium-sparing diuretics (triamterene, spironolactone, amiloride): avoid combining — can cause severe, life-threatening hyperkalemia
- ACE inhibitors and ARBs (common for blood pressure and heart failure): reduce potassium excretion; monitor blood levels closely
- NSAIDs (ibuprofen, naproxen, etc.): can reduce kidney clearance of potassium; monitor carefully
- Anticholinergic medications (used for bladder, GI, or other conditions): slow gut transit and can worsen GI irritation from solid potassium forms
- Digitalis (digoxin): rapid changes in potassium levels — either too high or too low — can trigger digitalis toxicity; extra caution and monitoring required
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Tell your prescriber if you have kidney disease or poor kidney function — potassium builds up and can reach dangerous levels
- Do not use potassium citrate tablets if you have hyperkalemia or conditions that raise potassium (chronic kidney failure, uncontrolled diabetes, adrenal insufficiency, severe dehydration, or are taking potassium-sparing drugs)
- Do not use potassium citrate tablets if you have peptic ulcer disease, an active urinary tract infection, or anything that slows movement through the gut (intestinal obstruction, esophageal compression, delayed stomach emptying, or use of anticholinergic drugs)
- Use with extreme caution if you have heart failure or severe heart muscle damage
- Pregnant women: potassium citrate should only be used if clearly needed — effects on the fetus are unknown
- Breastfeeding women: use potassium citrate only if clearly needed
- Children: safety and effectiveness of potassium citrate have not been established in pediatric patients
- Tell your doctor about all medications you take, especially diuretics, blood pressure drugs, and anti-inflammatory painkillers
🚑If you take too much▾
Too much potassium causes hyperkalemia, which can be life-threatening. Symptoms may include muscle weakness, paralysis, numbness or tingling, nausea, vomiting, low blood pressure, and dangerous heart rhythm disturbances — including cardiac arrest. Mild hyperkalemia is often symptomless and only detected on blood tests or an EKG. Any suspected potassium overdose or EKG changes suggesting hyperkalemia should be treated as a medical emergency — stop the potassium immediately and seek urgent medical care.
📡Pharmacodynamics — effects in the body▾
Potassium citrate raises the pH (acidity level) of urine and increases urinary citrate — a compound that binds to calcium and inhibits the formation of kidney stones. The rise in urinary pH also converts uric acid to a more soluble form, reducing uric acid stone formation. These combined effects make the urine a less favorable environment for calcium oxalate, calcium phosphate, and uric acid crystals to develop. With regular dosing, urine citrate rises within the first hour and stays elevated throughout the day, smoothing out the natural fluctuations that would otherwise allow stone-forming conditions to occur.
🔬Pharmacokinetics — how your body processes it▾
After a single oral dose of potassium citrate, urinary citrate begins to rise within the first hour and the effect lasts about 12 hours. With continued daily dosing, urinary citrate reaches its peak increase by about the third day of treatment. When treatment is stopped, urinary citrate begins falling back toward pre-treatment levels within the first day. The degree of citrate increase is directly related to the dose prescribed.
📦How to store it▾
Store in a tight container.
📄 Written from Potassium’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
Supplements & herbs that interact with Potassium
25 supplements and herbal products have documented interactions with Potassium in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 1
- Moderate · 14
- Minor · 10
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Potassium — the kind of thing our pharmacy team would talk through with you at the counter.
What's the difference between potassium chloride and potassium citrate — aren't they the same thing? ▾
Do I really need to dilute the liquid or powder form before I take it? ▾
What side effects should I actually worry about versus ones I can just watch? ▾
Can I take ibuprofen or other over-the-counter pain relievers while I'm on potassium? ▾
I'm pregnant — is it safe for me to take potassium citrate? ▾
My doctor wants me to get regular blood tests while I'm on this. Why is that necessary? ▾
Is Potassium available over the counter? ▾
When was Potassium first available? ▾
Who makes Potassium? ▾
💬 Answers drafted from Potassium’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Potassium comes
Potassium is available in 9 forms. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Extended-release tablet
Oral solution
Show 4 more strengths Show fewer strengths
Extended-release capsule
Other oral form
Show 7 more strengths Show fewer strengths
Tablet
Injection
Show 6 more strengths Show fewer strengths
Topical cream, ointment or gel
Topical solution
Sublingual tablet
📊 Potassium across the U.S. market
How Potassium appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (40) · Crystal (14) · Granule (4) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
📈 How widely Potassium is used
A general measure of how commonly Potassium is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Potassium is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Potassium prescribed? Of the 1,596 medications we measure, Potassium ranks #112 by Medicaid prescriptions — more than 93% of them.
Utilization by Potassium product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
Other Potassium products — combination packs and listings not yet matched to a specific clinical product (kept visible so every prescription is accounted for)
Summed across the 224 of 1,483 listed NDC products with Medicaid activity.
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Potassium, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 224 of 1,483 listed Potassium NDCs with Medicaid activity.
🔍 Compare Potassium products
A representative set of FDA-listed product records for Potassium — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Capsule | ||||
| 600 mg | — | Adare Pharmaceuticals Inc | DRUG FOR FURTHER PROCESSING | View NDC → |
| 600 mg | Oral | Adare Pharmaceuticals Inc × 2 listings | ANDA | View NDC → |
| 750 mg | — | Adare Pharmaceuticals Inc | DRUG FOR FURTHER PROCESSING | View NDC → |
| 750 mg | Oral | Adare Pharmaceuticals Inc × 2 listings | ANDA | View NDC → |
| 65 mg | Oral | Nature's Fusions, Llc | UNAPPROVED HOMEOPATHIC | View NDC → |
| 💊Extended-release capsule | ||||
| 750 mg | Oral | A-S Medication Solutions × 2 listings | ANDA | View NDC → |
| 10 mEq | Oral | A-S Medication Solutions × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | American Health Packaging × 3 listings | ANDA | View NDC → |
| 750 mg | Oral | Amneal Pharmaceuticals of New York LLC × 4 listings | ANDA | View NDC → |
| 750 mg | Oral | AvKARE × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | AvPAK × 3 listings | ANDA | View NDC → |
| 750 mg | Oral | BluePoint Laboratories × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Bryant Ranch Prepack × 6 listings | ANDA | View NDC → |
| 750 mg | Oral | Bryant Ranch Prepack × 6 listings | ANDA | View NDC → |
| 10 mEq | Oral | Cardinal Health | ANDA | View NDC → |
| 10 mEq | Oral | Cardinal Health 107, LLC | ANDA | View NDC → |
| 750 mg | Oral | Glenmark Pharmaceuticals Inc., USA × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Granules India Ltd × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | Granules India Ltd × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Granules Pharmaceuticals Inc × 3 listings | ANDA | View NDC → |
| 750 mg | Oral | Granules Pharmaceuticals Inc × 3 listings | ANDA | View NDC → |
| 8 mEq | Oral | Lupin Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 10 mEq | Oral | Lupin Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | Major Pharmaceuticals × 3 listings | ANDA | View NDC → |
| 10 mEq | Oral | Major Pharmaceuticals | ANDA | View NDC → |
| 750 mg | Oral | NCS HealthCare of KY, LLC dba Vangard Labs × 3 listings | ANDA | View NDC → |
| 10 mEq | Oral | NCS HealthCare of KY, LLC dba Vangard Labs | ANDA | View NDC → |
| 750 mg | Oral | Northstar Rx LLC × 2 listings | ANDA | View NDC → |
| 8 mEq | Oral | Novel Laboratories, Inc. | ANDA | View NDC → |
| 10 mEq | Oral | Novel Laboratories, Inc. | ANDA | View NDC → |
| 750 mg | Oral | NuCare Pharmaceuticals, Inc. | ANDA | Find on DailyMed ↗ |
| 8 mEq | Oral | NuCare Pharmaceuticals,Inc. | ANDA | Find on DailyMed ↗ |
| 750 mg | Oral | Padagis US LLC | ANDA | View NDC → |
| 600 mg | Oral | PD-Rx Pharmaceuticals, Inc. × 3 listings | ANDA | View NDC → |
| 750 mg | Oral | PD-Rx Pharmaceuticals, Inc. × 6 listings | ANDA | View NDC → |
| 10 mEq | Oral | RedPharm Drug, Inc. | ANDA | View NDC → |
| 750 mg | Oral | Remedyrepack Inc. × 5 listings | ANDA | View NDC → |
| 10 mEq | Oral | Remedyrepack Inc. × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Solco Healthcare LLC × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | Solco Healthcare LLC × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Sun Pharmaceutical Industries, Inc. × 2 listings | ANDA | View NDC → |
| 750 mg | Oral | Sun Pharmaceutical Industries, Inc. × 2 listings | ANDA | View NDC → |
| 600 mg | Oral | Upsher-Smith Laboratories, LLC | ANDA | View NDC → |
| 750 mg | Oral | Upsher-Smith Laboratories, LLC | ANDA | View NDC → |
| 600 mg | Oral | Zydus Pharmaceuticals (USA) Inc. | ANDA | View NDC → |
| 750 mg | Oral | Zydus Pharmaceuticals (USA) Inc. | ANDA | View NDC → |
| 💊Injection | ||||
| 7.46 g/1000 mL | Intravenous | Baxter Healthcare Corporation × 3 listings | NDA | View NDC → |
| 14.9 g/1000 mL | Intravenous | Baxter Healthcare Corporation × 3 listings | NDA | View NDC → |
| 29.8 g/1000 mL | Intravenous | Baxter Healthcare Corporation × 3 listings | NDA | View NDC → |
| 100 mEq/50 mL | Intravenous | Exela Pharma Sciences, LLC | ANDA | View NDC → |
| 200 mEq/100 mL | Intravenous | Exela Pharma Sciences, LLC | ANDA | View NDC → |
| 10 mEq/50 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 10 mEq/100 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 20 mEq/50 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 20 mEq/100 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 40 mEq/100 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 10 mEq/100 mL | Intravenous | ICU Medical Inc. × 4 listings | NDA | View NDC → |
| 200 mEq/1000 mL | Intravenous | ICU Medical Inc. × 3 listings | NDA | View NDC → |
| 400 mEq/1000 mL | Intravenous | ICU Medical Inc. × 2 listings | NDA | View NDC → |
| 7.45 mg/mL | Intravenous | Nexus Pharamaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 14.9 mg/mL | Intravenous | Nexus Pharamaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 29.8 mg/mL | Intravenous | Nexus Pharamaceuticals Inc. × 4 listings | ANDA | View NDC → |
| 💊Oral powder | ||||
| 1 [hp_X] | Oral | Seroyal USA × 2 listings | UNAPPROVED HOMEOPATHIC | View NDC → |
| 2 [hp_X] | Oral | Seroyal USA | UNAPPROVED HOMEOPATHIC | View NDC → |
| 3 [hp_X] | Oral | Seroyal USA | UNAPPROVED HOMEOPATHIC | View NDC → |
| 30 [kp_C] | Oral | Seroyal USA | UNAPPROVED HOMEOPATHIC | View NDC → |
| 💊Oral solution | ||||
| 1.5 g/1.58 g | Oral | Amneal Pharmaceuticals LLC | ANDA | View NDC → |
| 1.5 g/1.58 g | Oral | Amneal Pharmaceuticals NY LLC × 3 listings | ANDA | View NDC → |
| 1.5 g/1.56 g | Oral | ANI Pharmaceuticals, Inc. | ANDA | View NDC → |
| 1.5 g/1.58 g | Oral | Granules Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 3 g/3.16 g | Oral | IPG Pharmaceuticals, Inc. | NDA | View NDC → |
| 1.5 g/1.54 g | Oral | Lupin Pharmaceuticals,Inc. × 2 listings | ANDA | View NDC → |
| 1.5 g/1.54 g | Oral | Novel Laboratories, Inc. | ANDA | View NDC → |
| 1.5 g/1.58 g | Oral | Somerset Therapeutics, LLC | ANDA | View NDC → |
| 💊Topical cream, ointment or gel | ||||
| 5 g/100 g | Oral | 9055-7588 Qubec Inc. DBA Attitude | OTC MONOGRAPH DRUG | View NDC → |
| 5 g/100 g | Oral | Attitude DBA 9055-7588 Qu | OTC MONOGRAPH NOT FINAL | View NDC → |
| 5 g/100 g | Oral | Attitude DBA 9055-7588 Qu�bec Inc. | OTC MONOGRAPH NOT FINAL | View NDC → |
| 💊Bulk drug substance | ||||
| 1 kg/kg | — | Avantor Performance Materials, LLC × 6 listings | BULK INGREDIENT | View NDC → |
| 0.1 kg/0.1 kg | — | BioSpectra × 2 listings | BULK INGREDIENT | View NDC → |
| 0.5 kg/0.5 kg | — | BioSpectra × 2 listings | BULK INGREDIENT | View NDC → |
| 5 kg/5 kg | — | BioSpectra × 3 listings | BULK INGREDIENT | View NDC → |
| 10 kg/10 kg | — | BioSpectra × 3 listings | BULK INGREDIENT | View NDC → |
| 25 kg/25 kg | — | BioSpectra × 3 listings | BULK INGREDIENT | View NDC → |
| 100 mg | — | Coating Place, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 1 g/g | — | Holland Company, Inc. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Jost Chemical Co | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Jost Chemical Co. × 2 listings | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Jost Chemical Poland Sp Z O O × 2 listings | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Macco Organiques, S.r.o. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Merck KGaA | BULK INGREDIENT | View NDC → |
| 3 kg/3 kg | — | Merck KGaA | BULK INGREDIENT | View NDC → |
| 5 kg/5 kg | — | Merck KGaA | BULK INGREDIENT | View NDC → |
| 25 kg/25 kg | — | Merck KGaA | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Morton Salt, Inc. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Spectrum Laboratory Products, Inc. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Willow Birch Pharma, LLC | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
Showing 200 of 1,216 products — FDA National Drug Code Directory. See every product, package size and price: browse all 1,216 Potassium NDCs →
📈 What people report — real-world data (FDA FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Potassium — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Potassium in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
🏛️ The road to your pharmacy
How Potassium went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 Recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
Source: openFDA drug enforcement (recall) reports.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 8588 1 dose form · 1 strength
-
Dose form (SCDF) Oral Tablet RxCUI 373549In current FDA listingsClinical drug / strength (SCD) 80 MGRxCUI 259128
Look up RxCUI 8588 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
📦 Supply & shortage status
Whether Potassium is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
…and 16 more on the FDA NDC directory.
RxNorm drug class
Potassium belongs to the Sulfonamides and potassium in combination class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
🔬 Where this comes from
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 272 FDA-filed SPL label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
For canonical ingredient pages, bounded product-attributed indication and administration excerpts may be added to the AI evidence, and the generator is instructed to preserve available product, brand, route, and form qualifiers instead of treating one label as universal. Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. Biocomp Pharma, Inc. is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.