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Two medicines, side by side

Indapamide vs hydrochlorothiazide

Indapamide and hydrochlorothiazide are both labeled for high blood pressure, heart failure and edema (fluid retention). Drugs@FDA records approvals of indapamide since 1983 and of hydrochlorothiazide since 1959. Pharmacies paid $0.109 per indapamide 1.25 mg tablet and $0.0115 per hydrochlorothiazide 25 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Hydrochlorothiazide's other strengths are brand-only: $4.46 per mL (Inzirqo 10 mg/mL oral suspension). In FDA's classes, indapamide is a thiazide-like diuretic and hydrochlorothiazide a thiazide diuretic.

Check it at the source: the indapamide FDA label on DailyMed (effective October 1, 2022); the hydrochlorothiazide FDA label on DailyMed (effective June 12, 2026).

Highlights of the indapamide record

Indapamide (Lozol) · label of October 1, 2022

Used for

From the label: indications

Indapamide tablets are indicated for the treatment of hypertension, alone or in combination with other antihypertensive drugs. Indapamide tablets are also indicated for the treatment of salt and fluid retention associated with congestive heart failure. Usage in Pregnancy: The routine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unnecessary hazard (see PRECAUTIONS ). […]

On the market

Earliest approval on file
July 6, 1983
Generic labelers
8 labelers
Pharmacy cost
$0.109 per tablet

Supply and safety

Shortage
No current entry
Recalls
0

Highlights of the hydrochlorothiazide record

Hydrochlorothiazide (Inzirqo) · label of June 12, 2026

Used for

From the label: indications

Hydrochlorothiazide tablets USP are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Hydrochlorothiazide tablets USP have also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. […]

On the market

Earliest approval on file
February 12, 1959
Generic labelers
43 labelers
Pharmacy cost
$0.0115 per tablet

Supply and safety

Shortage
A presentation being discontinued
Recalls
7

Source: FDA drug labels via openFDA (Indapamide label of October 1, 2022, Hydrochlorothiazide label of June 12, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do indapamide and hydrochlorothiazide differ on the record?

In FDA's classes, indapamide is a thiazide-like diuretic and hydrochlorothiazide a thiazide diuretic.

Half-life, in each label's words: Indapamide, “The half-life of indapamide in whole blood is approximately 14 hours.”; Hydrochlorothiazide, “When plasma levels have been followed for at least 24 hours, the plasma half-life has been observed to vary between 5.6 …”

Generics: indapamide since 1995; hydrochlorothiazide since 1973 (Drugs@FDA).

IndapamideHydrochlorothiazide
Labeled forHigh blood pressure, Heart failure, Edema (fluid retention)Heart failure, High blood pressure, Edema (fluid retention)
Pharmacologic classThiazide-like DiureticThiazide Diuretic
How it works (label)n/an/a
Half-life (label)The half-life of indapamide in whole blood is approximately 14 hours.When plasma levels have been followed for at least 24 hours, the plasma half-life has been observed to vary between 5.6 and 14.8 hours.
Earliest approval on file (Drugs@FDA)July 6, 1983February 12, 1959
First generic approvedJuly 27, 1995January 12, 1973
Generic labelers (NDC)8 labelers43 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.109 per tablet (Indapamide 1.25 mg tablet)$0.0115 per tablet (Hydrochlorothiazide 25 mg tablet)
12-month price change+9%-7%
Boxed warningNoNo
Shortage nowNo current entryA presentation being discontinued
Recalls recorded07
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)17,817144,413
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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