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Two medicines, side by side

Bisoprolol vs olmesartan

Bisoprolol and olmesartan are both labeled for high blood pressure. Drugs@FDA records approvals of bisoprolol since 1992 and of olmesartan since 2002. Pharmacies paid $0.114 per bisoprolol fumarate 5 mg tablet and $0.0805 per olmesartan medoxomil 20 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. In FDA's classes, bisoprolol is a beta-adrenergic blocker and olmesartan an angiotensin 2 receptor blocker.

Check it at the source: the bisoprolol FDA label on DailyMed (effective March 11, 2026); the olmesartan FDA label on DailyMed (effective September 23, 2025).

Highlights of the bisoprolol record

Bisoprolol (Zebeta) · label of March 11, 2026

Used for

From the label: indications

Bisoprolol fumarate tablets are indicated in the management of hypertension. It may be used alone or in combination with other antihypertensive agents.

On the market

Earliest approval on file
July 31, 1992
Generic labelers
24 labelers
Pharmacy cost
$0.114 per tablet

Supply and safety

Shortage
No current entry
Recalls
2

Highlights of the olmesartan record

Olmesartan (Benicar) · label of September 23, 2025

Boxed warning

FETAL TOXICITY When pregnancy is detected, discontinue Benicar as soon as possible ( 5.1 , 8.1 ). Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus ( 5.1 , 8.1 ). WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning. When pregnancy is detected, discontinue Benicar as soon as possible ( 5.1 , 8.1 ).

Used for

From the label: indications

Benicar is indicated for the treatment of hypertension in adults and children six years of age and older, 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
April 25, 2002
Generic labelers
30 labelers
Pharmacy cost
$0.0805 per tablet

Supply and safety

Shortage
No current entry
Recalls
2

Source: FDA drug labels via openFDA (Bisoprolol label of March 11, 2026, Olmesartan label of September 23, 2025); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do bisoprolol and olmesartan differ on the record?

In FDA's classes, bisoprolol is a beta-adrenergic blocker and olmesartan an angiotensin 2 receptor blocker.

Half-life, in each label's words: Bisoprolol, “The plasma elimination half-life is 9 to 12 hours and is slightly longer in elderly patients, in part because of …”; Olmesartan, “Olmesartan appears to be eliminated in a biphasic manner with a terminal elimination half-life of approximately 13 …”

Only the olmesartan label carries a boxed warning.

Generics: bisoprolol since 2000; olmesartan since 2016 (Drugs@FDA).

BisoprololOlmesartan
Labeled forHigh blood pressureHigh blood pressure
Pharmacologic classbeta-Adrenergic BlockerAngiotensin 2 Receptor Blocker
How it works (label)n/aAngiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin converting enzyme (ACE, kininase II).
Half-life (label)The plasma elimination half-life is 9 to 12 hours and is slightly longer in elderly patients, in part because of decreased renal function in that population.Olmesartan appears to be eliminated in a biphasic manner with a terminal elimination half-life of approximately 13 hours.
Earliest approval on file (Drugs@FDA)July 31, 1992April 25, 2002
First generic approvedNovember 16, 2000October 26, 2016
Generic labelers (NDC)24 labelers30 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.114 per tablet (Bisoprolol fumarate 5 mg tablet)$0.0805 per tablet (Olmesartan medoxomil 20 mg tablet)
12-month price change-39%+1%
Boxed warningNoYes
Shortage nowNo current entryNo current entry
Recalls recorded22
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)135,06035,743
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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