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Two medicines, side by side

Nifedipine vs olmesartan

Nifedipine and olmesartan are both labeled for high blood pressure. Drugs@FDA records approvals of nifedipine since 1981 and of olmesartan since 2002. Pharmacies paid $0.130 per nifedipine ER 30 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, nifedipine is a dihydropyridine calcium channel blocker and olmesartan an angiotensin 2 receptor blocker.

Check it at the source: the nifedipine FDA label on DailyMed (effective December 24, 2024); the olmesartan FDA label on DailyMed (effective September 23, 2025).

Highlights of the nifedipine record

Nifedipine (Procardia) · label of December 24, 2024

Used for

From the label: indications

Nifedipine extended-release tablets are indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive agents.

On the market

Earliest approval on file
December 31, 1981
Generic labelers
32 labelers
Pharmacy cost
$0.130 per tablet

Supply and safety

Shortage
No current entry
Recalls
7

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 (Nifedipine label of December 24, 2024, Olmesartan label of September 23, 2025); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do nifedipine and olmesartan differ on the record?

In FDA's classes, nifedipine is a dihydropyridine calcium channel blocker and olmesartan an angiotensin 2 receptor blocker.

Half-life, in each label's words: Nifedipine, “The elimination half-life of nifedipine administered as nifedipine extended-release tablets are approximately 7 hours …”; 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: nifedipine since 1989; olmesartan since 2016 (Drugs@FDA).

NifedipineOlmesartan
Labeled forHigh blood pressure, AnginaHigh blood pressure
Pharmacologic classDihydropyridine Calcium Channel 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 elimination half-life of nifedipine administered as nifedipine extended-release tablets are approximately 7 hours in contrast to the known 2 hour elimination half-life of nifedipine administered as an immediate …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)December 31, 1981April 25, 2002
First generic approvedApril 28, 1989October 26, 2016
Generic labelers (NDC)32 labelers30 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.130 per tablet (Nifedipine ER 30 mg tablet)$0.0805 per tablet (Olmesartan medoxomil 20 mg tablet)
12-month price change+19%+1%
Boxed warningNoYes
Shortage nowNo current entryNo current entry
Recalls recorded72
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)41,05935,743
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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