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Two medicines, side by side

Captopril vs metoprolol

Captopril and metoprolol are both labeled for high blood pressure and heart failure. Drugs@FDA records approvals of captopril since 1981 and of metoprolol since 1978. Pharmacies paid $0.228 per captopril 12.5 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. Metoprolol's other strengths are brand-only: $1.20 per mL (Lopressor 10 mg/mL oral solution). In FDA's classes, captopril is an angiotensin converting enzyme inhibitor and metoprolol a beta-adrenergic blocker.

Check it at the source: the captopril FDA label on DailyMed (effective February 6, 2026); the metoprolol FDA label on DailyMed (effective March 3, 2026).

Highlights of the captopril record

Captopril (Capoten) · label of February 6, 2026

Boxed warning

FETAL TOXICITY When pregnancy is detected, discontinue captopril tablets as soon as possible. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. See WARNINGS: Fetal Toxicity

Used for

From the label: indications

Hypertension Captopril tablets are indicated for the treatment of hypertension. In using captopril tablets, consideration should be given to the risk of neutropenia/agranulocytosis (see WARNINGS ). Captopril tablets may be used as initial therapy for patients with normal renal function, in whom the risk is relatively low. […]

On the market

Earliest approval on file
April 6, 1981
Generic labelers
13 labelers
Pharmacy cost
$0.228 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 (Captopril label of February 6, 2026, Metoprolol label of March 3, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do captopril and metoprolol differ on the record?

In FDA's classes, captopril is an angiotensin converting enzyme inhibitor and metoprolol a beta-adrenergic blocker.

Half-life, in each label's words: Captopril, “The apparent elimination half-life for total radioactivity in blood is probably less than 3 hours.”; Metoprolol, “Elimination Elimination is mainly by biotransformation in the liver, and the plasma half-life ranges from approximately …”

Only the captopril label carries a boxed warning.

Generics: captopril since 1995; metoprolol since 1993 (Drugs@FDA).

CaptoprilMetoprolol
Labeled forHigh blood pressure, Heart failure, Chronic kidney diseaseHigh blood pressure, Angina, Heart failure, Heart attack and coronary artery disease
Pharmacologic classAngiotensin Converting Enzyme Inhibitorbeta-Adrenergic Blocker
How it works (label)n/aMetoprolol is a beta 1 -selective (cardioselective) adrenergic receptor blocking agent.
Half-life (label)The apparent elimination half-life for total radioactivity in blood is probably less than 3 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 6, 1981August 7, 1978
First generic approvedMarch 31, 1995December 21, 1993
Generic labelers (NDC)13 labelers74 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.228 per tablet (Captopril 12.5 mg tablet)$0.085 per tablet (Metoprolol succ ER 100 mg tablet)
12-month price change-28%-8%
Boxed warningYesNo
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)9,557353,609
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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