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Two medicines, side by side

Felodipine vs losartan

Felodipine and losartan are both labeled for high blood pressure. Drugs@FDA records approvals of felodipine since 1991 and of losartan since 1995. Pharmacies paid $0.123 per felodipine ER 5 mg tablet and $0.0327 per losartan potassium 50 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. In FDA's classes, felodipine is a dihydropyridine calcium channel blocker and losartan an angiotensin 2 receptor blocker.

Check it at the source: the felodipine FDA label on DailyMed (effective August 11, 2026); the losartan FDA label on DailyMed (effective January 20, 2026).

Highlights of the felodipine record

Felodipine (Plendil) · label of August 11, 2026

Used for

From the label: indications

Felodipine extended-release tablets, USP are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including felodipine. […]

On the market

Earliest approval on file
July 25, 1991
Generic labelers
14 labelers
Pharmacy cost
$0.123 per tablet

Supply and safety

Shortage
No current entry
Recalls
3

Highlights of the losartan record

Losartan (Cozaar) · label of January 20, 2026

Boxed warning

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

Used for

From the label: indications

COZAAR is an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure in adults and children greater than 6 years old. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Reduction of the risk of stroke in patients with hypertension and left ventricular hypertrophy. […]

On the market

Earliest approval on file
April 14, 1995
Generic labelers
43 labelers
Pharmacy cost
$0.0327 per tablet

Supply and safety

Shortage
No current entry
Recalls
77

Source: FDA drug labels via openFDA (Felodipine label of August 11, 2026, Losartan label of January 20, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do felodipine and losartan differ on the record?

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

Only the losartan label carries a boxed warning.

Generics: felodipine since 2004; losartan since 2010 (Drugs@FDA).

FelodipineLosartan
Labeled forHigh blood pressureHigh blood pressure, Chronic kidney disease, Stroke prevention
Pharmacologic classDihydropyridine Calcium Channel BlockerAngiotensin 2 Receptor Blocker
How it works (label)n/aAngiotensin II [formed from angiotensin I in a reaction catalyzed by angiotensin converting enzyme (ACE, kininase II)] is a potent vasoconstrictor, the primary vasoactive hormone of the renin-angiotensin system, and an important component …
Half-life (label)n/aThe terminal half-life of losartan is about 2 hours and of the metabolite is about 6-9 hours.
Earliest approval on file (Drugs@FDA)July 25, 1991April 14, 1995
First generic approvedNovember 2, 2004April 6, 2010
Generic labelers (NDC)14 labelers43 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.123 per tablet (Felodipine ER 5 mg tablet)$0.0327 per tablet (Losartan potassium 50 mg tablet)
12-month price change-27%+2%
Boxed warningNoYes
Shortage nowNo current entryNo current entry
Recalls recorded377
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)11,323200,566
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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