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Medication guide

Bisoprolol: uses, appearance and warnings

What the official FDA label says Bisoprolol is used for, what it looks like, and its most important warnings — in plain English, with the label text one click away.
beta-Adrenergic BlockerPrescription label

Uses

What the official label says Bisoprolol is used for

The FDA label for Bisoprolol states:

Bisoprolol fumarate tablets are indicated in the management of hypertension. It may be used alone or in combination with other antihypertensive agents.
Read the label's “Indications and usage” section (verbatim)
Bisoprolol fumarate tablets are indicated in the management of hypertension. It may be used alone or in combination with other antihypertensive agents.

Names & forms

Brand names, forms and strengths

We did not find brand names for this exact product in RxNorm. Ask your pharmacist which brand or generic version you have.

Generic name: bisoprolol · RxNorm ID (RxCUI): 19484

Forms and strengths of Bisoprolol listed in RxNorm
FormStrengths listed in RxNorm
Oral Tablet1.25 MG, 2.5 MG, 3.75 MG, 5 MG, 7.5 MG, 10 MG

Strengths are listed so you can recognise a product — not as dosing information. Only your prescriber can decide what is right for you.

Appearance

What Bisoprolol looks like

Illustration: pink round tablet, film coated, imprint II

bisoprolol fumarate 5 mg
Micro Labs Limited

Illustration: white round tablet, film coated, imprint IIII

bisoprolol fumarate 10 mg
Micro Labs Limited

Illustration: white round tablet, film coated, imprint UpArrowhead H1UpArrowhead H1

bisoprolol fumarate 2.5 mg
Advagen Pharma Ltd

Illustration: Peach round tablet, film coated, imprint UpArrowhead F1UpArrowhead F1

bisoprolol fumarate 5 mg
Advagen Pharma Ltd

Illustration: white round tablet, film coated, imprint UpArrowhead F2UpArrowhead F2

bisoprolol fumarate 10 mg
Advagen Pharma Ltd

Illustration: pink round tablet, film coated, imprint FCFC

bisoprolol fumarate 5 mg
Rising Pharma Holdings, Inc.

Illustration based on label data — not a photo; appearance varies by manufacturer. Confirm with your pharmacist.
Appearance of Bisoprolol products from DailyMed product data
StrengthFormColourShapeSizeImprintScoreLabeler
bisoprolol fumarate 5 mgtablet, film coatedpinkround6 mmI2Micro Labs Limited
bisoprolol fumarate 10 mgtablet, film coatedwhiteround7 mmII1Micro Labs Limited
bisoprolol fumarate 2.5 mgtablet, film coatedwhiteround6 mmUpArrowhead · H11Advagen Pharma Ltd
bisoprolol fumarate 5 mgtablet, film coatedpink“Peach”round7 mmUpArrowhead · F12Advagen Pharma Ltd
bisoprolol fumarate 10 mgtablet, film coatedwhiteround7 mmUpArrowhead · F21Advagen Pharma Ltd
bisoprolol fumarate 5 mgtablet, film coatedpinkround6 mmFC2Rising Pharma Holdings, Inc.
bisoprolol fumarate 10 mgtablet, film coatedwhite“White to off white colored”round7 mmFE1Rising Pharma Holdings, Inc.

From the product data in each manufacturer's label on DailyMed. Many companies make Bisoprolol, so your medicine may look different from any shown here. If a pill looks unfamiliar, ask your pharmacist before taking it.

Read the label's “How supplied” section (verbatim)
Bisoprolol fumarate tablets, USP are supplied as 5 mg and 10 mg tablets. The 5 mg tablets are pink, round-shaped, film-coated tablets, with deep score-line on one side and convex with ' ǀ ' debossed on other side. They are supplied as follows: Bottles of 30 Unit-of-use with child-resistant closure: NDC 42571-470-30 Bottles of 100 with child-resistant closure: NDC 42571-470-01 Bottles of 500: NDC 42571-470-05 The 10 mg tablets are white to off-white, round, biconvex film-coated tablets debossed with ' ǀ ǀ ' on one side and plain on other side. They are supplied as follows: Bottles of 30 Unit-of-use with child-resistant closure: NDC 42571-471-30 Bottles of 100 with child-resistant closure: NDC 42571-471-01 Bottles of 500: NDC 42571-471-05 Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect from moisture. Dispense in tight, light-resistant containers. Manufactured by: Micro Labs Limited Goa-403 722, INDIA Manufactured for: Micro Labs USA, Inc. Somerset, NJ 08873 Rev. 09/2023

Safety

Important warnings for Bisoprolol

Cardiac Failure Sympathetic stimulation is a vital component supporting circulatory function in the setting of congestive heart failure, and beta-blockade may result in further depression of myocardial contractility and precipitate more severe failure. In general, beta-blocking agents should be avoided in patients with overt congestive failure. However, in some patients with compensated cardiac failure it may be necessary to utilize them. In such a situation, they must be used cautiously. …

Contraindications — who should not use it (verbatim)
Bisoprolol fumarate tablets are contraindicated in patients with cardiogenic shock, overt cardiac failure, second or third degree AV block, and marked sinus bradycardia.
Warnings and precautions (verbatim excerpt)
Cardiac Failure Sympathetic stimulation is a vital component supporting circulatory function in the setting of congestive heart failure, and beta-blockade may result in further depression of myocardial contractility and precipitate more severe failure. In general, beta-blocking agents should be avoided in patients with overt congestive failure. However, in some patients with compensated cardiac failure it may be necessary to utilize them. In such a situation, they must be used cautiously. In Patients Without a History of Cardiac Failure Continued depression of the myocardium with beta-blockers can, in some patients, precipitate cardiac failure. At the first signs or symptoms of heart failure, discontinuation of bisoprolol fumarate should be considered. In some cases, beta-blocker therapy can be continued while heart failure is treated with other drugs. Abrupt Cessation of Therapy Exacerbation of angina pectoris, and, in some instances, myocardial infarction or ventricular arrhythmia, have been observed in patients with coronary artery disease following abrupt cessation of therapy with beta-blockers. Such patients should, therefore, be cautioned against interruption or discontinuation of therapy without the physician’s advice. Even in patients without overt coronary artery disease, it may be advisable to taper therapy with bisoprolol fumarate over approximately one week with the patient under careful observation. If withdrawal symptoms occur, bisoprolol fumarate therapy should be reinstituted, at least temporarily. Peripheral Vascular Disease Beta-blockers can precipitate or aggravate symptoms of arterial insufficiency in patients with peripheral vascular disease. Caution should be exercised in such individuals. Bronchospastic Disease PATIENTS WITH BRONCHOSPASTIC DISEASE SHOULD, IN GENERAL, NOT RECEIVE BETA-BLOCKERS. Because of its relative beta 1 -selectivity, however, bisoprolol fumarate may be used with caution in patients with bronchospastic disease who do not respond to, or who cannot tolerate other antihypertensive treatment. Since beta 1 -selectivity is not absolute, the lowest possible dose of bisoprolol fumarate should be used, with therapy starting at 2.5 mg. A beta 2 agonist (bronchodilator) should be made available. Major Surgery Chronically administered beta-blocking therapy should not be routinely withdrawn prior to major surgery; however, the impaired ability of the heart to respond to reflex adrenergic stimuli may augment the risks of general anesthesia and surgical procedures. Diabetes and Hypoglycemia Beta-blockers may mask some of the manifestations of hypoglycemia, particularly tachycardia. Nonselective beta-blockers may potentiate insulin-induced hypoglycemia and delay recovery of serum glucose levels. Because of its beta 1 -selectivity, this is less likely with bisoprolol fumarate. However, patients subject to spontaneous hypoglycemia, or diabetic patients receiving insulin or oral hypoglycemic agents, should be cautioned about these possibilities and bisoprolol fumarate should be used with caution. Thyrotoxicosis Beta-adrenergic blockade may mask clinical signs of hyperthyroidism, such as tachycardia. Abrupt withdrawal of beta-blockade may be followed by an exacerbation of the symptoms of hyperthyroidism or may precipitate thyroid storm.
Side effects — opening of the label's adverse reactions section
Safety data are available in more than 30,000 patients or volunteers. Frequency estimates and rates of withdrawal of therapy for adverse events were derived from two U.S. placebo-controlled studies. In Study A, doses of 5, 10, and 20 mg bisoprolol fumarate were administered for 4 weeks. In Study B, doses of 2.5, 10, and 40 mg of bisoprolol fumarate were administered for 12 weeks. A total of 273 patients were treated with 5 to 20 mg of bisoprolol fumarate; 132 received placebo. Withdrawal of therapy for adverse events was 3.3% for patients receiving bisoprolol fumarate and 6.8% for patients on placebo. Withdrawals were less than 1% for either bradycardia or fatigue/lack of energy. …
Drug interactions — opening of the label's section
Bisoprolol fumarate should not be combined with other beta-blocking agents. Patients receiving catecholamine-depleting drugs, such as reserpine or guanethidine, should be closely monitored, because the added beta-adrenergic blocking action of bisoprolol fumarate may produce excessive reduction of sympathetic activity. In patients receiving concurrent therapy with clonidine, if therapy is to be discontinued, it is suggested that bisoprolol fumarate be discontinued for several days before the withdrawal of clonidine. Bisoprolol fumarate should be used with care when myocardial depressants or inhibitors of AV conduction, such as certain calcium antagonists (particularly of the phenylalkylamine [verapamil] and benzothiazepine [diltiazem] classes), or antiarrhythmic agents, such as disopyramide, are used concurrently. …

This is not a complete list of warnings or side effects. Read the full label and talk to your prescriber or pharmacist. To report a side effect to the FDA, use MedWatch.

Resources

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Sources

Label text is quoted from the Micro Labs Limited label (label version effective March 11, 2026), retrieved October 20, 2026. Other manufacturers' labels for the same medicine may differ in wording.

If anything here differs from the label that came with your medicine, follow your label and your pharmacist.

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