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Two medicines, side by side

Nifedipine vs telmisartan

Nifedipine and telmisartan are both labeled for high blood pressure. Drugs@FDA records approvals of nifedipine since 1981 and of telmisartan since 1998. Pharmacies paid $0.130 per nifedipine ER 30 mg tablet and $0.106 per telmisartan 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 telmisartan an angiotensin 2 receptor blocker.

Check it at the source: the nifedipine FDA label on DailyMed (effective December 24, 2024); the telmisartan FDA label on DailyMed (effective May 29, 2026).

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 telmisartan record

Telmisartan (Micardis) · label of May 29, 2026

Boxed warning

FETAL TOXICITY When pregnancy is detected, discontinue telmisartan as soon as possible [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1)]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1)]. WARNING: FETAL TOXICITY See full prescribing information for complete boxed warnings.

Used for

From the label: indications

Telmisartanis an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions(1.1) 1.1 Hypertension Telmisartan is indicated for the treatment of hypertension, to lower blood pressure. […]

On the market

Earliest approval on file
November 10, 1998
Generic labelers
28 labelers
Pharmacy cost
$0.106 per tablet

Supply and safety

Shortage
No current entry
Recalls
3

Source: FDA drug labels via openFDA (Nifedipine label of December 24, 2024, Telmisartan label of May 29, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do nifedipine and telmisartan differ on the record?

In FDA's classes, nifedipine is a dihydropyridine calcium channel blocker and telmisartan 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 …”; Telmisartan, “Telmisartan shows bi-exponential decay kinetics with a terminal elimination half-life of approximately 24 hours.”

Only the telmisartan label carries a boxed warning.

Generics: nifedipine since 1989; telmisartan since 2014 (Drugs@FDA).

NifedipineTelmisartan
Labeled forHigh blood pressure, AnginaHigh blood pressure, Heart attack and coronary artery disease
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 …Telmisartan shows bi-exponential decay kinetics with a terminal elimination half-life of approximately 24 hours.
Earliest approval on file (Drugs@FDA)December 31, 1981November 10, 1998
First generic approvedApril 28, 1989January 8, 2014
Generic labelers (NDC)32 labelers28 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.130 per tablet (Nifedipine ER 30 mg tablet)$0.106 per tablet (Telmisartan 20 mg tablet)
12-month price change+19%-4%
Boxed warningNoYes
Shortage nowNo current entryNo current entry
Recalls recorded73
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)41,05917,745
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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