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Molecule

Atenolol

Beta-Adrenergic Blocker
Available on requestCardiology
Presentations
6
Brands
1
Manufacturers
1
Available from stock
0

Atenolol is a beta-adrenergic blocker indicated for the treatment of hypertension, to lower blood pressure, among other approved uses. It is available as tablets for oral use. MedsAcross supplies Atenolol 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, Adrenergic beta-Antagonists
ATC classification
C07AB03 Atenolol · Beta blockers, subgroup C07A, subgroup C07AB
US FDA first approval
19 August 1981
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
Identifiers
UNII 50VV3VW0TIRxCUI 1202CAS 29122-68-7DrugBank DB00335Q411325

Clinical information

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

Uses

Hypertension TENORMIN is 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. 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

Hypertension The initial dose of TENORMIN is 50 mg given as one tablet a day either alone or added to diuretic therapy. The full effect of this dose will usually be seen within one to two weeks. If an optimal response is not achieved, the dosage should be increased to TENORMIN 100 mg given as one tablet a day. Increasing the dosage beyond 100 mg a day is unlikely to produce any further benefit. TENORMIN may be used alone or concomitantly with other antihypertensive agents including thiazide-type diuretics, hydralazine, prazosin, and alpha-methyldopa. Angina Pectoris The initial dose of TENORMIN is 50 mg given as one tablet a day. If an optimal response is not achieved within one week, the dosage should be increased to TENORMIN 100 mg given as one tablet a day. Some patients may require a dosage of 200 mg once a day for optimal effect.

Source: US FDA prescribing information

Contraindications

TENORMIN is contraindicated in sinus bradycardia, heart block greater than first degree, cardiogenic shock, and overt cardiac failure. TENORMIN is contraindicated in those patients with a history of hypersensitivity to the atenolol or any of the drug product’s components.

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 with acute myocardial infarction, cardiac failure which is not promptly and effectively controlled by 80 mg of intravenous furosemide or equivalent therapy is a contraindication to beta-blocker treatment. 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.

Source: US FDA prescribing information

Side effects

Most adverse effects have been mild and transient. The frequency estimates in the following table were derived from controlled studies in hypertensive patients 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 TENORMIN and placebo-treated patients than when these reactions were volunteered. Where frequency of adverse effects of TENORMIN and placebo is similar, causal relationship to TENORMIN is uncertain. Volunteered (US Studies) Total − Volunteered and Elicited (Foreign + US Studies) Atenolol (n=164) % Placebo (n=206) % Atenolol (n=399) % Placebo (n=407) % CARDIOVASCULAR Bradycardia 3 0 3 0 Cold Extremities 0 0.5 12 5 Postural Hypotension 2 1 4 5 Leg Pain 0 0.5 3 1 CENTRAL NERVOUS SYSTEM/ NEUROMUSCULAR Dizziness 4 1 13 6 Vertigo 2 0.5 2

Source: US FDA prescribing information

Interactions

Catecholamine-depleting drugs (e.g., reserpine) may have an additive effect when given with beta-blocking agents. Patients treated with TENORMIN plus a catecholamine depletor should therefore 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 TENORMIN. 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. Beta-blockers may exacerbate the rebound hypertension which can follow the withdrawal of clonidine.

Source: US FDA prescribing information

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

All presentations

6 presentations of Atenolol, sorted by availability.

MedicineManufacturerRegisterAvailability
Atenolol 25 mg tabletOralGeneric name—US FDAAvailable on request
Atenolol 50 mg tabletOralGeneric name—US FDAAvailable on request
Atenolol 100 mg tabletOralGeneric name—US FDAAvailable on request
Tenormin 100 mg tabletOralUpsher-Smith LaboratoriesUS FDAAvailable on request
Tenormin 25 mg tabletOralUpsher-Smith LaboratoriesUS FDAAvailable on request
Tenormin 50 mg tabletOralUpsher-Smith LaboratoriesUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

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 19 August 1981Drugs@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 in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Atenolol available for export from India?

Yes, on request. MedsAcross lists 6 presentations of Atenolol and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Atenolol have?

The catalogue lists 1 brand names for Atenolol, including Tenormin.

Is Atenolol approved by the US FDA?

Yes. The US FDA first approved Atenolol on 19 August 1981, according to Drugs@FDA.

Does Atenolol need cold chain shipping?

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

Which ATC class is Atenolol in?

Atenolol is classified under ATC code C07AB03 (Atenolol).

References

  1. TENORMIN prescribing information (Upsher-Smith Laboratories). U.S. National Library of Medicine, DailyMed. Retrieved 18 September 2025

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