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Two medicines, side by side

Chlorthalidone vs metoprolol

Chlorthalidone and metoprolol are both labeled for high blood pressure and heart failure. Drugs@FDA records approvals of chlorthalidone since 1960 and of metoprolol since 1978. Pharmacies paid $0.0743 per chlorthalidone 25 mg tablet and $0.085 per metoprolol succ ER 100 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Chlorthalidone's other strengths are brand-only: $0.957 per Hemiclor 12.5 mg tablet. Metoprolol's other strengths are brand-only: $1.20 per mL (Lopressor 10 mg/mL oral solution). In FDA's classes, chlorthalidone is a thiazide-like diuretic and metoprolol a beta-adrenergic blocker.

Check it at the source: the chlorthalidone FDA label on DailyMed (effective August 5, 2026); the metoprolol FDA label on DailyMed (effective March 3, 2026).

Highlights of the chlorthalidone record

Chlorthalidone (Hygroton) · label of August 5, 2026

Used for

From the label: indications

Diuretics such as chlorthalidone are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension. Chlorthalidone is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. […]

On the market

Earliest approval on file
April 7, 1960
Generic labelers
36 labelers
Pharmacy cost
$0.0743 per tablet

Supply and safety

Shortage
No current entry
Recalls
5

Highlights of the metoprolol record

Metoprolol (Lopressor) · label of March 3, 2026

Used for

From the label: indications

TOPROL-XL, metoprolol succinate, is a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Angina Pectoris. […]

On the market

Earliest approval on file
August 7, 1978
Generic labelers
74 labelers
Pharmacy cost
$0.085 per tablet

Supply and safety

Shortage
A presentation being discontinued
Recalls
39

Source: FDA drug labels via openFDA (Chlorthalidone label of August 5, 2026, Metoprolol label of March 3, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do chlorthalidone and metoprolol differ on the record?

In FDA's classes, chlorthalidone is a thiazide-like diuretic and metoprolol a beta-adrenergic blocker.

Half-life, in each label's words: Chlorthalidone, “The mean half-life following a 50 to 200 mg dose is 40 hours.”; Metoprolol, “Elimination Elimination is mainly by biotransformation in the liver, and the plasma half-life ranges from approximately …”

Generics: chlorthalidone since 1981; metoprolol since 1993 (Drugs@FDA).

ChlorthalidoneMetoprolol
Labeled forHigh blood pressure, Heart failure, Edema (fluid retention)High blood pressure, Angina, Heart failure, Heart attack and coronary artery disease
Pharmacologic classThiazide-like Diureticbeta-Adrenergic Blocker
How it works (label)n/aMetoprolol is a beta 1 -selective (cardioselective) adrenergic receptor blocking agent.
Half-life (label)The mean half-life following a 50 to 200 mg dose is 40 hours.Elimination Elimination is mainly by biotransformation in the liver, and the plasma half-life ranges from approximately 3 to 7 hours.
Earliest approval on file (Drugs@FDA)April 7, 1960August 7, 1978
First generic approvedFebruary 26, 1981December 21, 1993
Generic labelers (NDC)36 labelers74 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0743 per tablet (Chlorthalidone 25 mg tablet)$0.085 per tablet (Metoprolol succ ER 100 mg tablet)
12-month price change-12%-8%
Boxed warningNoNo
Shortage nowNo current entryA presentation being discontinued
Recalls recorded539
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)11,545353,609
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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