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Two medicines, side by side

Amlodipine vs metoprolol

Amlodipine and metoprolol are both labeled for high blood pressure, angina and heart attack and coronary artery disease. Drugs@FDA records approvals of amlodipine since 1992 and of metoprolol since 1978. Pharmacies paid $0.0102 per amlodipine besylate 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, amlodipine is a calcium channel blocker and metoprolol a beta-adrenergic blocker.

Check it at the source: the amlodipine FDA label on DailyMed (effective February 15, 2023); the metoprolol FDA label on DailyMed (effective March 3, 2026).

Highlights of the amlodipine record

Amlodipine (Norvasc) · label of February 15, 2023

Used for

From the label: indications

NORVASC is a calcium channel blocker and may be used alone or in combination with other antihypertensive and antianginal agents for the treatment of: • Hypertension ( 1.1 ) o NORVASC is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. […]

On the market

Earliest approval on file
July 31, 1992
Generic labelers
42 labelers
Pharmacy cost
$0.0102 per tablet

Supply and safety

Shortage
No current entry
Recalls
30

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 (Amlodipine label of February 15, 2023, Metoprolol label of March 3, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do amlodipine and metoprolol differ on the record?

In FDA's classes, amlodipine is a calcium channel blocker and metoprolol a beta-adrenergic blocker.

How each works, in its label's words: Amlodipine, “Amlodipine is a dihydropyridine calcium antagonist (calcium ion antagonist or slow‑channel blocker) that inhibits the transmembrane influx of calcium ions into vascular smooth muscle and cardiac …”; Metoprolol, “Metoprolol is a beta 1 -selective (cardioselective) adrenergic receptor blocking agent.”

Generics: amlodipine since 2005; metoprolol since 1993 (Drugs@FDA).

AmlodipineMetoprolol
Labeled forHigh blood pressure, Angina, Heart attack and coronary artery diseaseHigh blood pressure, Angina, Heart failure, Heart attack and coronary artery disease
Pharmacologic classCalcium Channel Blocker, Dihydropyridine Calcium Channel Blockerbeta-Adrenergic Blocker
How it works (label)Amlodipine is a dihydropyridine calcium antagonist (calcium ion antagonist or slow‑channel blocker) that inhibits the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle.Metoprolol is a beta 1 -selective (cardioselective) adrenergic receptor blocking agent.
Half-life (label)n/aElimination 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)July 31, 1992August 7, 1978
First generic approvedOctober 3, 2005December 21, 1993
Generic labelers (NDC)42 labelers74 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0102 per tablet (Amlodipine besylate 5 mg tablet)$0.085 per tablet (Metoprolol succ ER 100 mg tablet)
12-month price change-10%-8%
Boxed warningNoNo
Shortage nowNo current entryA presentation being discontinued
Recalls recorded3039
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)409,186353,609
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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