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Two medicines, side by side

Atenolol vs carvedilol

Atenolol and carvedilol are both labeled for high blood pressure. Drugs@FDA records approvals of atenolol since 1981 and of carvedilol since 1995. Pharmacies paid $0.0217 per atenolol 25 mg tablet and $0.0179 per carvedilol 6.25 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. In FDA's classes, atenolol is a beta-adrenergic blocker and carvedilol an alpha-adrenergic blocker.

Check it at the source: the atenolol FDA label on DailyMed (effective September 18, 2025); the carvedilol FDA label on DailyMed (effective July 31, 2026).

Highlights of the atenolol record

Atenolol (Tenormin) · label of September 18, 2025

Used for

From the label: indications

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. […]

On the market

Earliest approval on file
August 19, 1981
Generic labelers
35 labelers
Pharmacy cost
$0.0217 per tablet

Supply and safety

Shortage
No current entry
Recalls
4

Highlights of the carvedilol record

Carvedilol (Coreg) · label of July 31, 2026

Used for

From the label: indications

INDICATIONS AND USAGE COREG is an alpha-/beta-adrenergic blocking agent indicated for the treatment of: mild to severe chronic heart failure ( 1.1 ) left ventricular dysfunction following myocardial infarction in clinically stable patients ( 1.2 ) hypertension ( 1.3 ) 1.1 Heart Failure COREG is indicated for the treatment of mild-to-severe chronic heart failure of ischemic or cardiomyopathic origin, usually in […]

On the market

Earliest approval on file
September 14, 1995
Generic labelers
41 labelers
Pharmacy cost
$0.0179 per tablet

Supply and safety

Shortage
No current entry
Recalls
22

Source: FDA drug labels via openFDA (Atenolol label of September 18, 2025, Carvedilol label of July 31, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do atenolol and carvedilol differ on the record?

In FDA's classes, atenolol is a beta-adrenergic blocker and carvedilol an alpha-adrenergic blocker.

Half-life, in each label's words: Atenolol, “The elimination half-life of oral TENORMIN is approximately 6 to 7 hours, and there is no alteration of the kinetic …”; Carvedilol, “Following oral administration, the apparent mean terminal elimination half-life of carvedilol generally ranges from 7 …”

Generics: atenolol since 1988; carvedilol since 2007 (Drugs@FDA).

AtenololCarvedilol
Labeled forHigh blood pressure, Angina, Heart attack and coronary artery diseaseHeart failure, High blood pressure
Pharmacologic classbeta-Adrenergic Blockeralpha-Adrenergic Blocker, beta-Adrenergic Blocker
How it works (label)n/aCOREG is a racemic mixture in which nonselective β-adrenoreceptor blocking activity is present in the S(-) enantiomer and α1-adrenergic blocking activity is present in both R(+) and S(-) enantiomers at equal potency.
Half-life (label)The elimination half-life of oral TENORMIN is approximately 6 to 7 hours, and there is no alteration of the kinetic profile of the drug by chronic administration.Following oral administration, the apparent mean terminal elimination half-life of carvedilol generally ranges from 7 to 10 hours.
Earliest approval on file (Drugs@FDA)August 19, 1981September 14, 1995
First generic approvedJuly 15, 1988September 5, 2007
Generic labelers (NDC)35 labelers41 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0217 per tablet (Atenolol 25 mg tablet)$0.0179 per tablet (Carvedilol 6.25 mg tablet)
12-month price change-3%-4%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded422
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)132,491137,029
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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