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Fixed-dose combination

Atenolol and Chlorthalidone

Also known as atenolol, chlorthalidone
Available on request
Presentations
2
Brands
0
Manufacturers
0
Available from stock
0

Atenolol and Chlorthalidone is a fixed-dose combination of a thiazide-like diuretic and a beta-adrenergic blocker indicated for the treatment of hypertension, to lower blood pressure. It is available as tablets for oral use. MedsAcross supplies Atenolol and Chlorthalidone 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

Key facts

Pharmacological class
Beta-Adrenergic Blocker, Thiazide-like Diuretic, Adrenergic beta-Antagonists, Increased Diuresis
US FDA first approval
8 June 1984
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet
Fixed-dose combination of
Atenolol, Chlorthalidone
Identifiers
RxCUI 151195Q7700570

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

Atenolol and chlorthalidone tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including atenolol and chlorthalidone. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals.

Source: US FDA prescribing information

Dosing overview

DOSAGE MUST BE INDIVIDUALIZED. Chlorthalidone is usually given at a dose of 25 mg daily, the usual initial dose of atenolol is 50 mg daily. Therefore, the initial dose should be one atenolol and chlorthalidone 50mg/25mg tablet given once a day. If an optimal response is not achieved, the dosage should be increased to one atenolol and chlorthalidone 100mg/25mg tablet given once a day. When necessary, another antihypertensive agent may be added gradually beginning with 50 percent of the usual recommended starting dose to avoid an excessive fall in blood pressure. Since atenolol is excreted via the kidneys, dosage should be adjusted in cases of severe impairment of renal function.

Source: US FDA prescribing information

Contraindications

Atenolol and chlorthalidone tablets are contraindicated in patients with: sinus bradycardia, heart block greater than first degree, cardiogenic shock, overt cardiac failure, anuria, hypersensitivity to this product or to sulfonamide-derived drugs.

Source: US FDA prescribing information

Warnings and precautions

Cardiac Failure Sympathetic stimulation is necessary in supporting circulatory function in congestive heart failure, and beta blockade carries the potential hazard of further depressing myocardial contractility and precipitating more severe failure. IN PATIENTS WITHOUT A HISTORY OF CARDIAC FAILURE, continued depression of the myocardium with beta-blocking agents over a period of time can, in some cases, lead to cardiac failure. At the first sign or symptom of impending cardiac failure, patients should be treated appropriately according to currently recommended guidelines, and the response observed closely. If cardiac failure continues despite adequate treatment, atenolol and chlorthalidone tablets should be withdrawn.

Source: US FDA prescribing information

Side effects

Atenolol and chlorthalidone tablets are usually well tolerated in properly selected patients. Most adverse effects have been mild and transient. The adverse effects observed for atenolol and chlorthalidone tablets are essentially the same as those seen with the individual components. Atenolol The frequency estimates in the following table were derived from controlled studies in which adverse reactions were either volunteered by the patient (US studies) or elicited, e.g., by checklist (foreign studies). The reported frequency of elicited adverse effects was higher for both atenolol and placebo-treated patients than when these reactions were volunteered. Where frequency of adverse effects for atenolol and placebo is similar, causal relationship to atenolol is uncertain.

Source: US FDA prescribing information

Interactions

Atenolol and chlorthalidone tablets may potentiate the action of other antihypertensive agents used concomitantly. Patients treated with atenolol and chlorthalidone tablets plus a catecholamine depletor (e.g., reserpine) should be closely observed for evidence of hypotension and/or marked bradycardia which may produce vertigo, syncope or postural hypotension. Calcium channel blockers may also have an additive effect when given with atenolol and chlorthalidone tablets. Disopyramide is a Type I antiarrhythmic drug with potent negative inotropic and chronotropic effects. Disopyramide has been associated with severe bradycardia, asystole and heart failure when administered with beta-blockers. Amiodarone is an antiarrhythmic agent with negative chronotropic properties that may be additive to those seen with beta-blockers. Thiazides may decrease arterial responsiveness to norepinephrine.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

2 presentations of Atenolol and Chlorthalidone, sorted by availability.

MedicineActive ingredientManufacturerRegisterAvailability
Atenolol and Chlorthalidone 100 mg/25 mg tabletOralGeneric nameAtenolol and Chlorthalidone—US FDAAvailable on request
Atenolol and Chlorthalidone 50 mg/25 mg tabletOralGeneric nameAtenolol and Chlorthalidone—US FDAAvailable on request

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 8 June 1984Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Atenolol and Chlorthalidone in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Atenolol and Chlorthalidone available for export from India?

Yes, on request. MedsAcross lists 2 presentations of Atenolol and Chlorthalidone and sources them for licensed hospitals, importers and physicians against valid import documents.

Is Atenolol and Chlorthalidone approved by the US FDA?

Yes. The US FDA first approved Atenolol and Chlorthalidone on 8 June 1984, according to Drugs@FDA.

Does Atenolol and Chlorthalidone need cold chain shipping?

No listed presentation of Atenolol and Chlorthalidone is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

References

  1. Atenolol and Chlorthalidone prescribing information (Northstar Rx). U.S. National Library of Medicine, DailyMed. Retrieved 5 October 2026

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