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Two medicines, side by side

Captopril vs clonidine

Captopril and clonidine are both labeled for high blood pressure. Drugs@FDA records approvals of captopril since 1981 and of clonidine since 1974. Pharmacies paid $0.228 per captopril 12.5 mg tablet and $0.0241 per clonidine HCl 0.1 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Clonidine's other strengths are brand-only: $1.53 per mL (Javadin 0.02 mg/mL solution). In FDA's classes, captopril is an angiotensin converting enzyme inhibitor and clonidine a central alpha-2 adrenergic agonist.

Check it at the source: the captopril FDA label on DailyMed (effective February 6, 2026); the clonidine FDA label on DailyMed (effective March 30, 2026).

Highlights of the captopril record

Captopril (Capoten) · label of February 6, 2026

Boxed warning

FETAL TOXICITY When pregnancy is detected, discontinue captopril tablets as soon as possible. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. See WARNINGS: Fetal Toxicity

Used for

From the label: indications

Hypertension Captopril tablets are indicated for the treatment of hypertension. In using captopril tablets, consideration should be given to the risk of neutropenia/agranulocytosis (see WARNINGS ). Captopril tablets may be used as initial therapy for patients with normal renal function, in whom the risk is relatively low. […]

On the market

Earliest approval on file
April 6, 1981
Generic labelers
13 labelers
Pharmacy cost
$0.228 per tablet

Supply and safety

Shortage
No current entry
Recalls
5

Highlights of the clonidine record

Clonidine (Catapres) · label of March 30, 2026

Used for

From the label: indications

Clonidine hydrochloride tablets are indicated in the treatment of hypertension. Clonidine hydrochloride tablets may be employed alone or concomitantly with other antihypertensive agents.

On the market

Earliest approval on file
September 3, 1974
Generic labelers
43 labelers
Pharmacy cost
$0.0241 per tablet

Supply and safety

Shortage
No current entry
Recalls
16

Source: FDA drug labels via openFDA (Captopril label of February 6, 2026, Clonidine label of March 30, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do captopril and clonidine differ on the record?

In FDA's classes, captopril is an angiotensin converting enzyme inhibitor and clonidine a central alpha-2 adrenergic agonist.

Half-life, in each label's words: Captopril, “The apparent elimination half-life for total radioactivity in blood is probably less than 3 hours.”; Clonidine, “Following intravenous administration, clonidine displays biphasic disposition with a distribution half-life of about 20 …”

Only the captopril label carries a boxed warning.

Generics: captopril since 1995; clonidine since 1986 (Drugs@FDA).

CaptoprilClonidine
Labeled forHigh blood pressure, Heart failure, Chronic kidney diseaseHigh blood pressure, ADHD, Pain
Pharmacologic classAngiotensin Converting Enzyme InhibitorCentral alpha-2 Adrenergic Agonist
How it works (label)n/an/a
Half-life (label)The apparent elimination half-life for total radioactivity in blood is probably less than 3 hours.Following intravenous administration, clonidine displays biphasic disposition with a distribution half-life of about 20 minutes and an elimination half-life ranging from 12 to 16 hours.
Earliest approval on file (Drugs@FDA)April 6, 1981September 3, 1974
First generic approvedMarch 31, 1995July 1, 1986
Generic labelers (NDC)13 labelers43 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.228 per tablet (Captopril 12.5 mg tablet)$0.0241 per tablet (Clonidine HCl 0.1 mg tablet)
12-month price change-28%-3%
Boxed warningYesNo
Shortage nowNo current entryNo current entry
Recalls recorded516
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)9,55757,116
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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