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Metoprolol: uses, dosing, side effects & brands

Metoprolol is a beta-adrenergic blocker sold in the U.S. under 5 brand and generic names, for angina pectoris, atrial fibrillation and atrial flutter. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.

By the pharmaranks editorial teamReviewed against the FDA (openFDA label, NDC Directory & Enforcement) sourcesUpdated Jul 24, 2026How we research

Key facts

Drug class
Beta-Adrenergic Blocker
Treats (across its forms)
Angina Pectoris, Atrial Fibrillation and Atrial Flutter
Available as
Injectable · Solution · Tablet · Capsule, extended release · Tablet, extended release
Sold as
5 products — Metoprolol Tartrate, Kapspargo Sprinkle and Lopressor, and others
Prescription?
Prescription only
Generic available?
Yes
Half-life
about 3 to 4 hours
What the pharmacy pays
about $0.58 for a 30-count supply — not your price

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How Kapspargo Sprinkle is dosed

From the FDA label for Kapspargo Sprinkle (application NDA210428). Other metoprolol products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.

Adult Hypertension: Usual initial dosage is 25 to 100 mg once daily. Titrate weekly (or longer) to optimal blood pressure. (2.1) • Pediatric Hypertension 6 years of age and older: The recommended starting dose is 1 mg/kg, once daily and titrate to response. Do not exceed a maximum initial dose of 50 mg once daily. (2.1) • Angina Pectoris: Usual initial dosage is 100 mg once daily. Titrate weekly based on clinical response. (2.2) • Heart Failure: The recommended starting dose is 25 mg doubled every two weeks to the highest dose tolerated or up to 200 mg. (2.3) 2.1 Hypertension Adults: The usual initial dosage is 25 mg to 100 mg once daily in a single dose. Adjust dosage at weekly (or longer) intervals until optimum blood pressure reduction is achieved. Dosages above 400 mg per day have not been studied. Pediatric Hypertensive Patients 6 Years of age or older: The recommended starting dose of metoprolol succinate extended-release capsules is 1 mg/kg once daily, the maximum initial dose should not exceed 50 mg once daily. Adjust dosage according to blood pressure response. Doses above 2 mg/kg (or in excess of 200 mg) once daily have not been studied in pediatric patients [see Clinical Pharmacology (12.3)]. Metoprolol succinate extended-release capsules has not been studied in pediatric patients less than 6 years of age [see Use in Specific Populations (8.4)] . 2.2 Angina Pectoris…

Everything below is the FDA label for Kapspargo Sprinkle (capsule, extended release). Metoprolol is also sold as injectable, solution, tablet and tablet, extended release, and those are different medicines to take — follow the label for the one you were prescribed.

Kapspargo Sprinkle side effects

The following adverse reactions are described elsewhere in labeling: • Worsening angina or myocardial infarction. [see Warnings and Precautions (5)] • Worsening heart failure. [see Warnings and Precautions (5)] • Worsening AV block. [see Contraindications (4)] • Most common adverse reactions: tiredness, dizziness, depression, shortness of breath, bradycardia, hypotension, diarrhea, pruritus, rash. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Sun Pharmaceutical Industries, Inc. at 1-800-406-7984 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The adverse reaction information from clinical trials does, however, provide a basis for identifying the adverse events that appear to be related to drug use and for approximating rates. Hypertension and Angina: Most adverse reactions have been mild and transient. The most common (>2%) adverse reactions are tiredness, dizziness, depression, diarrhea, shortness of breath, bradycardia, and rash. Heart Failure: In the MERIT-HF study comparing metoprolol succinate in daily doses up to 200 mg (mean dose 159 mg once-daily; n=1990) to placebo…

Who shouldn’t take Kapspargo Sprinkle

Metoprolol succinate is contraindicated in severe bradycardia, second or third degree heart block, cardiogenic shock, decompensated heart failure, sick sinus syndrome (unless a permanent pacemaker is in place), and in patients who are hypersensitive to any component of this product. • Known hypersensitivity to product components. (4) • Severe bradycardia, greater than first degree heart block, or sick sinus syndrome without a pacemaker. (4) • Cardiogenic shock or decompensated heart failure. (4)

Kapspargo Sprinkle drug interactions

Catecholamine-depleting drugs may have an additive effect when given with beta-blocking agents. (7.1) • Patients may be unresponsive to the usual doses of epinephrine used to treat allergic reaction. (7.2) • CYP2D6 Inhibitors are likely to increase metoprolol concentration. (7.3) • Concomitant use of glycosides, clonidine, and diltiazem and verapamil with beta-blockers can increase the risk of bradycardia. (7.4) • Beta-blockers including metoprolol, may exacerbate the rebound hypertension that can follow the withdrawal of clonidine. (7.4) • Alcohol interferes with the extended release properties of this product. (7.5) 7.1 Catecholamine Depleting Drugs Catecholamine depleting drugs (e.g., reserpine, monoamine oxidase (MAO) inhibitors) may have an additive effect when given with beta-blocking agents. Observe patients treated with metoprolol succinate plus a catecholamine depletor for evidence of hypotension or marked bradycardia, which may produce vertigo, syncope, or postural hypotension. 7.2 Epinephrine While taking beta-blockers, patients with a history of severe anaphylactic reactions to a variety of allergens may be more reactive to repeated challenge and may be unresponsive to the usual doses of epinephrine used to treat an allergic reaction. 7.3 CYP2D6 Inhibitors Drugs that are strong inhibitors of CYP2D6, such as quinidine, fluoxetine, paroxetine, and propafenone, were shown to double metoprolol concentrations. While there is no information about moderate or weak inhibitors, these too are likely to increase metoprolol concentration. Increases in plasma concentration decrease the cardioselectivity of metoprolol [see Clinical Pharmacology (12.3)]. Monitor patients closely, when the combination cannot be avoided. 7.4 Digitalis, Clonidine, and Calcium Channel Blockers Digitalis glycosides, clonidine, diltiazem and verapamil slow atrioventricular conduction and decrease heart rate. Concomitant use with beta blockers can increase the risk of bradycardia. If clonidine and a beta blocker, such as metoprolol are coadministered, withdraw the beta-blocker several days before the gradual withdrawal of clonidine because beta-blockers may exacerbate the rebound hypertension that can follow the withdrawal of clonidine. If replacing clonidine by beta-blocker therapy, delay the introduction of beta-blockers for several days after clonidine administration has stopped . 7.5 Alcohol Metoprolol succinate is released faster from metoprolol succinate extended-release capsules in the presence of alcohol. This may increase the risk for adverse events associated with metoprolol succinate extended-release capsules. Avoid alcohol consumption when taking metoprolol succinate extended-release capsules [see Clinical Pharmacology (12.3)].

Can you take metoprolol with…?

Source-cited answers for the combinations people actually ask about — each with a verdict and what to watch for.

Every metoprolol product we track (5)

Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.

Metoprolol products
#DrugRatingPharmacy pays
160/100$1View →
2Not yet rated$1View →
3Not yet rated$1View →
4Not yet rated$1View →
5Not yet rated$1View →

What metoprolol pills look like

Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.

Metoprolol pill imprints
ImprintStrengthColourShape
R5050 mgpinkround
L;15150 mgpinkround
5;67200 mgwhiteoval
C;L;40750 mgwhiteround
566100 mgwhiteround
M;3whiteround
M;1825 mgwhiteround
M;3250 mgpinkround
A;3whiteoval
A50whiteround
A100whiteround
A200whiteoval

Combination products containing metoprolol

A combination is a different drug — different dosing, different warnings. It is listed here so you can find it, not so you can substitute it.

Metoprolol recalls

From the FDA Enforcement database. A recall covers specific lots — not the drug as a whole.

Can you crush or split metoprolol?

At least one metoprololproduct is labelled to be swallowed whole — crushing an extended-release tablet releases the whole day’s dose at once. Which applies depends on the form you were given.

What each metoprolol label says about crushing, splitting and chewing

How long metoprolol keeps

No metoprolol label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.

Does metoprolol expire? The in-use limits and storage rules from its labels

Metoprolol and breastfeeding

From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.

Because of the low levels of metoprolol in breastmilk, amounts ingested by the infant are small and would not be expected to cause any adverse effects in breastfed infants. Studies on the use of metoprolol during breastfeeding have found no adverse reactions in breastfed infants. Monitor breastfed infants for symptoms of beta blockade such as bradycardia and listlessness due to hypoglycemia.

Full LactMed record for metoprolol: levels in milk, effects in breastfed infants, and the drugs it would consider instead

National Institute of Child Health and Human Development, record revised November 15, 2024. LactMed states its information is not a substitute for professional judgement.

What people report to the FDA about metoprolol

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 68,291 reports naming metoprolol, and the FDA flagged 68% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • fatigue4,851 reports
  • diarrhoea4,079 reports
  • nausea3,968 reports
  • dyspnoea3,910 reports
  • dizziness3,169 reports
  • asthenia2,862 reports
  • headache2,579 reports
  • fall2,453 reports

Read these as a signal, not a rate. A report does not mean metoprolol caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.

Source: openFDA drug/event (FAERS), retrieved August 25, 2026.

How long metoprolol stays in your system

The elimination half-life of metoprolol is about 3 to 4 hours. This is for immediate-release metoprolol tartrate; the half-life is longer (about 7 to 9 hours) in the roughly 8% of people who are poor CYP2D6 metabolizers, so it varies with how a person metabolizes the drug. Metoprolol's metabolites have no meaningful beta-blocking activity, so no active metabolite extends the effect.

Metoprolol Tartrate tablet, film coated — DailyMed

Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.

Related calculators

Frequently asked questions

What is Kapspargo Sprinkle?

Metoprolol succinate, is a beta 1 -selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release capsules. Metoprolol succinate extended-release capsules have been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The extended-release capsules comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets. Each pellet acts as a separate drug delivery unit and is designed to deliver metoprolol continuously over the dosage interval.

What kind of drug is metoprolol?

The FDA classifies metoprolol as a beta-adrenergic blocker. Beta-blockers block adrenaline (epinephrine) and noradrenaline from acting on beta-adrenergic receptors, mainly in the heart. This slows the heart rate, reduces how forcefully the heart contracts, and lowers blood pressure, easing the workload on the heart. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.

How long does metoprolol stay in your system?

The elimination half-life of metoprolol is about 3 to 4 hours — that is how long the body takes to clear half of a dose. This is for immediate-release metoprolol tartrate; the half-life is longer (about 7 to 9 hours) in the roughly 8% of people who are poor CYP2D6 metabolizers, so it varies with how a person metabolizes the drug. Metoprolol's metabolites have no meaningful beta-blocking activity, so no active metabolite extends the effect. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.

Can you take metoprolol with other medicines?

It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run metoprolol against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.

What brand names is metoprolol sold under?

We track 5 metoprolol-containing products in the U.S.: Metoprolol Tartrate, Kapspargo Sprinkle, Lopressor, Metoprolol Succinate and Toprol-XL. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.

What forms does metoprolol come in?

Across the brands we track, metoprolol is currently marketed as injectable, solution, tablet, capsule, extended release and tablet, extended release, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.

Is there a generic metoprolol?

Yes. Our catalog lists 2 generic metoprolol products alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.

Has metoprolol been recalled?

The FDA's Enforcement database lists at least 5 recall records whose product description mentions metoprolol. The most recent: Metoprolol Succinate Extended-Release Tablets (Jan 29, 2026). A recall applies to specific lots, not to the drug as a whole — check the record for the affected lot numbers.

How long does it take for metoprolol to work?

Metoprolol slows the heart rate within a couple of hours of a dose, but its full blood-pressure effect builds over about 1 to 2 weeks of regular use. Do not stop it suddenly — abruptly stopping a beta blocker can cause a rebound in heart rate and blood pressure.

What should I avoid while taking metoprolol?

Other medicines: we hold source-cited interaction answers for Can you take Eliquis and metoprolol together?. This is what the FDA label and our cited sources say — it is not a complete list. Your pharmacist can check your own combination.

What are the common side effects of Lopressor / Toprol XL (metoprolol)?

The most common side effects of metoprolol (brand names Lopressor and Toprol XL) come from its beta-blocking action, which slows the heart and lowers blood pressure. MedlinePlus lists tiredness, dizziness or lightheadedness, diarrhea, dry mouth, and rash or itching. Because it slows heart rate, many people also notice a slower pulse, cold hands and feet, low blood pressure, and sometimes depressed mood, unusually vivid dreams, or trouble sleeping. Most of these are mild and often ease over the first few weeks. This is not a complete list — check the label or your pharmacist for others.

What serious side effects of metoprolol (Lopressor / Toprol XL) mean I should call a doctor or go to the ER?

Get medical help right away for signs the drug is slowing your heart too much or worsening heart failure. MedlinePlus says to seek immediate attention for: “Shortness of breath or difficulty breathing; swelling of the hands, feet, ankles, or lower legs; weight gain; fainting; rapid, pounding, or irregular heartbeat.” Fainting or a very slow pulse can mean dangerous bradycardia, and new swelling or breathlessness can signal worsening heart failure. If you have asthma or other lung disease, metoprolol can trigger wheezing or bronchospasm — tell your doctor before starting and seek care if breathing gets worse.

Can I stop taking Lopressor / Toprol XL (metoprolol) if I feel fine or have side effects?

No — never stop metoprolol on your own. Stopping a beta blocker suddenly is itself dangerous. MedlinePlus warns plainly: “If you suddenly stop taking metoprolol you may experience serious heart problems.” Abrupt withdrawal can cause rebound chest pain (angina), a heart attack, or dangerous heart rhythms, especially in people with heart disease. If you and your doctor decide to stop, the dose must be lowered gradually — the FDA label advises tapering over about one to two weeks under medical supervision. Keep taking it even when you feel well, and talk to your prescriber about any bothersome effects instead of quitting.

Does metoprolol (Lopressor / Toprol XL) hide low blood sugar warning signs in diabetes?

Yes — this is an important issue if you have diabetes. Metoprolol can both increase the risk of hypoglycemia and blunt the warning signs your body normally gives. MedlinePlus states it “may increase the risk of hypoglycemia (low blood sugar) and prevent the warning signs and symptoms that would tell you that your blood sugar is low” — beta blockers can mask the fast or pounding heartbeat you'd usually feel when sugar drops (though sweating still tends to occur). If you take insulin or diabetes medicines, monitor your blood sugar more closely and ask your doctor how to spot lows while on metoprolol.

When do metoprolol (Lopressor / Toprol XL) side effects start and how long do they last?

Early side effects such as tiredness, dizziness, and a slower heart rate often appear within the first hours to days as your body adjusts to the lower heart rate and blood pressure, and they commonly fade over a few weeks. Fatigue, cold hands and feet, or vivid dreams may linger for some people; if they don't settle or interfere with daily life, tell your prescriber — the dose or formulation may be adjusted. Do not stop the drug to make side effects go away, since sudden withdrawal risks serious heart problems (MedlinePlus). This describes typical patterns, not every possible reaction.

Cite this page
APA
pharmaranks. (2026, July 24). Metoprolol: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/metoprolol
MLA
“Metoprolol: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/metoprolol.

We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.

Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.

Read the full FDA label for metoprolol on DailyMed (NIH) ↗.