Hydrochlorothiazide: uses, dosing, side effects & brands
Hydrochlorothiazide is a thiazide diuretic sold in the U.S. under 5 brand and generic names, for edema, heart failure and hypertension. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
Key facts
- Drug class
- Thiazide Diuretic
- Treats (across its forms)
- Edema, Heart Failure and Hypertension
- Available as
- Capsule · Tablet · Powder
- Sold as
- 5 products — Hydrochlorothiazide, Oretic and Esidrix, and others
- Prescription?
- Prescription only
- Generic available?
- Yes
- Half-life
- about 6 to 15 hours (the label reports a range, not a single number)
- What the pharmacy pays
- about $0.90 for a 30-count supply — not your price
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How Hydrochlorothiazide is dosed
From the FDA label for Hydrochlorothiazide (application ANDA090510). Other hydrochlorothiazide products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
For Control of Hypertension: The adult initial dose of hydrochlorothiazide capsules is one capsule given once daily whether given alone or in combination with other antihypertensives. Total daily doses greater than 50 mg are not recommended.
Everything below is the FDA label for Hydrochlorothiazide (capsule, tablet). Hydrochlorothiazide is also sold as powder, and those are different medicines to take — follow the label for the one you were prescribed.
Hydrochlorothiazide side effects
The adverse reactions associated with hydrochlorothiazide have been shown to be dose related. In controlled clinical trials, the adverse events reported with doses of 12.5 mg hydrochlorothiazide once daily were comparable to placebo. The following adverse reactions have been reported for doses of hydrochlorothiazide 25 mg and greater and, within each category, are listed in the order of decreasing severity. Body as a whole: Weakness. Cardiovascular: Hypotension including orthostatic hypotension (may be aggravated by alcohol, barbiturates, narcotics or antihypertensive drugs). Digestive: Pancreatitis, jaundice (intrahepatic cholestatic jaundice), diarrhea, vomiting, sialadenitis, cramping, constipation, gastric irritation, nausea, anorexia. Hematologic: Aplastic anemia, agranulocytosis, leukopenia, hemolytic anemia, thrombocytopenia. Hypersensitivity: Anaphylactic reactions, necrotizing angiitis (vasculitis and cutaneous vasculitis), respiratory distress including pneumonitis and pulmonary edema, photosensitivity, fever, urticaria, rash, purpura. Metabolic: Electrolyte imbalance (see PRECAUTIONS ), hyperglycemia, glycosuria, hyperuricemia. Musculoskeletal: Muscle Spasm. Nervous System/Psychiatric: Vertigo, paresthesia, dizziness, headache, restlessness. Renal : Renal failure, renal dysfunction, interstitial nephritis (see WARNINGS ). Skin: Erythema multiforme including…
Who shouldn’t take Hydrochlorothiazide
Hydrochlorothiazide capsules are contraindicated in patients with anuria. Hypersensitivity to this product or other sulfonamide derived drugs is also contraindicated.
Hydrochlorothiazide drug interactions
When given concurrently the following drugs may interact with thiazide diuretics: Alcohol, barbiturates, or narcotics – potentiation of orthostatic hypotension may occur. Antidiabetic drugs – (oral agents and insulin) dosage adjustment of the antidiabetic drug may be required. Other antihypertensive drugs – additive effect or potentiation. Cholestyramine and colestipol resins – Cholestyramine and colestipol resins bind the hydrochlorothiazide and reduce its absorption from the gastrointestinal tract by up to 85 and 43 percent, respectively. Corticosteroid, ACTH – intensified electrolyte depletion, particularly hypokalemia. Pressor amines (e.g., norepinephrine) – possible decreased response to pressor amines but not sufficient to preclude their use. Skeletal muscle relaxants, nondepolarizing (e.g., tubocurarine) – possible increased responsiveness to the muscle relaxant. Lithium – generally should not be given with diuretics. Diuretic agents reduce the renal clearance of lithium and greatly increase the risk of lithium toxicity. Refer to the package insert for lithium preparations before use of such preparations with hydrochlorothiazide. Non-steroidal anti-inflammatory drugs – In some patients, the administration of a non-steroidal anti-inflammatory agent can reduce the diuretic, natriuretic, and antihypertensive effects of loop, potassium-sparing and thiazide diuretics. When hydrochlorothiazide and non-steroidal anti-inflammatory agents are used concomitantly, the patients should be observed closely to determine if the desired effect of the diuretic is obtained. Drug/Laboratory Test Interactions – Thiazides should be discontinued before carrying out tests for parathyroid function (see PRECAUTIONS , General). Carcinogenesis, Mutagenesis, Impairment of Fertility: Two-year feeding studies in mice and rats conducted under the auspices of the National Toxicology Program (NTP) uncovered no evidence of a carcinogenic potential of hydrochlorothiazide in female mice (at doses of up to approximately 600 mg/kg/day) or in male and female rats (at doses of approximately 100 mg/kg/day). The NTP, however, found equivocal evidence for hepatocarcinogenicity in male mice. Hydrochlorothiazide was not genotoxic in vitro in the Ames mutagenicity assay of Salmonella typhimurium strains TA 98, TA 100, TA 1535, TA 1537, and TA 1538 and in the Chinese Hamster Ovary (CHO) test for chromosomal aberrations, or in vivo in assays using mouse germinal cell chromosomes, Chinese hamster bone marrow chromosomes, and the Drosophila sex-linked recessive lethal trait gene. Positive test results were obtained only in the in vitro CHO Sister Chromatid Exchange (clastogenicity) and in the Mouse Lymphoma Cell (mutagenicity) assays, using concentrations of hydrochlorothiazide from 43 to 1,300 mcg/mL, and in the Aspergillus nidulans non-disjunction assay at an unspecified concentration. Hydrochlorothiazide had no adverse effects on the fertility of mice and rats of either sex in studies wherein these species were exposed, via their diet, to doses of up to 100 and 4 mg/kg, respectively, prior to conception and throughout gestation.
Every hydrochlorothiazide product we track (5)
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
| # | Drug | Rating | Type | Form | Generic? | Pharmacy pays | |
|---|---|---|---|---|---|---|---|
| 1 | 72/100 | Prescription | Capsule | Generic | $1 | View → | |
| 2 | 72/100 | Prescription | Tablet | Generic | $1 | View → | |
| 3 | 70/100 | Prescription | Tablet | Generic | $1 | View → | |
| 4 | 70/100 | Prescription | Suspension | Generic | $1 | View → | |
| 5 | Not yet rated | Prescription | Capsule | Generic | $1 | View → |
What hydrochlorothiazide pills look like
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
| Imprint | Strength | Colour | Shape | Maker |
|---|---|---|---|---|
| P;172 | 5 mg / 160 mg / 12.5 mg | white | oval | — |
| P;174 | 10 mg / 160 mg / 12.5 mg | brown | oval | — |
| P;173 | 5 mg / 160 mg / 25 mg | yellow | oval | — |
| P;175 | 10 mg / 25 mg / 320 mg | white | oval | — |
| P;185 | 10 mg / 25 mg / 160 mg | yellow | oval | — |
| P;172 | 5 mg / 160 mg / 12.5 mg | white | oval | — |
| P;174 | 10 mg / 160 mg / 12.5 mg | brown | oval | — |
| P;173 | 5 mg / 160 mg / 25 mg | yellow | oval | — |
| P;175 | 10 mg / 25 mg / 320 mg | white | oval | — |
| P;185 | 10 mg / 25 mg / 160 mg | yellow | oval | — |
| SG;146 | 12.5 mg | white | capsule | — |
| U;128 | 25 mg | orange | round | — |
Combination products containing hydrochlorothiazide
A combination is a different drug — different dosing, different warnings. It is listed here so you can find it, not so you can substitute it.
Hydrochlorothiazide recalls
From the FDA Enforcement database. A recall covers specific lots — not the drug as a whole.
Bisoprolol Fumarate and Hydrochlorothiazide tablets
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
Unichem Pharmaceuticals USA Inc. · Jan 21, 2026
Bisoprolol Fumarate and Hydrochlorothiazide Tablets
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
Glenmark Pharmaceuticals Inc., USA · Nov 21, 2025
Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg
Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
Lupin Pharmaceuticals Inc. · Jun 20, 2025
Losartan Potassium and Hydrochlorothiazide Tablets
Presence of foreign substance: plastic-like substance.
MACLEODS PHARMA USA, INC · May 7, 2024
How long hydrochlorothiazide keeps
No hydrochlorothiazide label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.
Does hydrochlorothiazide expire? The in-use limits and storage rules from its labelsHydrochlorothiazide and breastfeeding
From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.
Full LactMed record for hydrochlorothiazide: levels in milk, effects in breastfed infants, and the drugs it would consider insteadHydrochlorothiazide doses of 50 mg daily or less are acceptable during lactation. Intense diuresis with large doses may decrease breastmilk production.
National Institute of Child Health and Human Development, record revised September 15, 2025. LactMed states its information is not a substitute for professional judgement.
What people report to the FDA about hydrochlorothiazide
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 215,975 reports naming hydrochlorothiazide, and the FDA flagged 68% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- fatigue14,752 reports
- nausea14,379 reports
- diarrhoea12,427 reports
- dyspnoea11,185 reports
- dizziness11,112 reports
- headache10,846 reports
- arthralgia8,432 reports
- asthenia8,400 reports
Read these as a signal, not a rate. A report does not mean hydrochlorothiazide caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.
Source: openFDA drug/event (FAERS), retrieved August 25, 2026.
How long hydrochlorothiazide stays in your system
The elimination half-life of hydrochlorothiazide is about 6 to 15 hours (the label reports a range, not a single number). This is the plasma ELIMINATION half-life. Plasma levels fall bi-exponentially: other FDA labels for hydrochlorothiazide combination products describe a distribution phase of roughly 2 hours before the ~10-hour (6-15 h) elimination phase — the elimination figure is the one given here. Hydrochlorothiazide is NOT a prodrug and is NOT metabolized, so there is no active metabolite that outlasts the parent; more than 95% of the absorbed dose is excreted unchanged in urine. Kidney impairment: the label states plainly that in patients with renal disease plasma concentrations are increased and the elimination half-life is PROLONGED — it does not quantify by how much. The label does not state a different half-life for older adults or for liver impairment, so no number should be assumed for those groups. Absorption (not elimination) is reduced in congestive heart failure. This is a pharmacokinetic figure about how long the drug stays in plasma; it is not a drug-test detection window and not dosing guidance.
DailyMed — HYDROCHLOROTHIAZIDE capsule, Clinical Pharmacology (Pharmacokinetics and Metabolism) ↗Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.
Related calculators
Frequently asked questions
What is Hydrochlorothiazide?
Hydrochlorothiazide is a thiazide diuretic used to treat Edema, Heart Failure, Hypertension, Nephrotic Syndrome.
What kind of drug is hydrochlorothiazide?
The FDA classifies hydrochlorothiazide as a thiazide diuretic. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.
How long does hydrochlorothiazide stay in your system?
The elimination half-life of hydrochlorothiazide is about 6 to 15 hours (the label reports a range, not a single number) — that is how long the body takes to clear half of a dose. This is the plasma ELIMINATION half-life. Plasma levels fall bi-exponentially: other FDA labels for hydrochlorothiazide combination products describe a distribution phase of roughly 2 hours before the ~10-hour (6-15 h) elimination phase — the elimination figure is the one given here. Hydrochlorothiazide is NOT a prodrug and is NOT metabolized, so there is no active metabolite that outlasts the parent; more than 95% of the absorbed dose is excreted unchanged in urine. Kidney impairment: the label states plainly that in patients with renal disease plasma concentrations are increased and the elimination half-life is PROLONGED — it does not quantify by how much. The label does not state a different half-life for older adults or for liver impairment, so no number should be assumed for those groups. Absorption (not elimination) is reduced in congestive heart failure. This is a pharmacokinetic figure about how long the drug stays in plasma; it is not a drug-test detection window and not dosing guidance. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.
Can you take hydrochlorothiazide with other medicines?
It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run hydrochlorothiazide against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.
What brand names is hydrochlorothiazide sold under?
We track 5 hydrochlorothiazide-containing products in the U.S.: Hydrochlorothiazide, Oretic, Esidrix, Inzirqo and Microzide. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.
What forms does hydrochlorothiazide come in?
Across the brands we track, hydrochlorothiazide is currently marketed as capsule, tablet and powder, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.
Is there a generic hydrochlorothiazide?
Yes. Our catalog lists 1 generic hydrochlorothiazide product alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.
Has hydrochlorothiazide been recalled?
The FDA's Enforcement database lists 4 recall records whose product description mentions hydrochlorothiazide. The most recent: Bisoprolol Fumarate and Hydrochlorothiazide tablets (Jan 21, 2026). A recall applies to specific lots, not to the drug as a whole — check the record for the affected lot numbers.
How long does it take for hydrochlorothiazide to work?
Hydrochlorothiazide starts its water-pill (diuretic) effect within about 2 hours, but its full blood-pressure-lowering effect develops over several weeks of daily use.
What are the common side effects of Microzide (hydrochlorothiazide)?
Because Microzide (hydrochlorothiazide) is a thiazide diuretic ("water pill"), the most common effect is passing more urine, especially in the first hours after a dose. MedlinePlus lists frequent urination, along with headache, loss of appetite, diarrhea, and hair loss. Many people also feel dizzy or lightheaded, particularly when standing up quickly, because the drug lowers blood volume and blood pressure. Hydrochlorothiazide also tends to lower blood potassium and to nudge blood sugar and uric acid upward — low potassium can show up as muscle cramps or weakness. These effects are dose-dependent and more common above 25 mg per day (StatPearls). Mild dizziness or extra urination usually does not need urgent care, but tell your prescriber if it is bothersome.
When should Microzide (hydrochlorothiazide) side effects be treated as an emergency?
Call your doctor right away or seek emergency care for signs of serious electrolyte imbalance or dehydration. MedlinePlus lists "dry mouth; thirst; nausea; vomiting; weakness, tiredness; drowsiness; restlessness; confusion; muscle weakness, pain, or cramps; fast heartbeat and other signs of dehydration and electrolyte imbalance." Hydrochlorothiazide can lower potassium, sodium, and magnesium (StatPearls), and severe drops can trigger dangerous heart rhythms. Also get urgent help for "difficulty breathing or swallowing," "blisters or peeling skin," hives, or ongoing stomach pain that spreads to the back (possible pancreatitis). This list is not complete — treat any severe or fast-worsening symptom as a reason to call.
Can Microzide (hydrochlorothiazide) cause sudden vision problems or eye pain?
Yes, and it is a medical emergency. MedlinePlus says to call your doctor immediately for "changes in vision, eye pain, or swelling or redness in or around the eye." Hydrochlorothiazide is a sulfonamide, and StatPearls notes that "rare cases of acute myopia and secondary angle-closure glaucoma have been reported, typically within days of therapy initiation." This means sudden blurred or worsening nearsightedness and eye pain can appear within hours to weeks of starting the drug. Untreated acute angle-closure glaucoma can permanently damage vision, so do not wait — seek same-day eye care and tell them you take hydrochlorothiazide.
Does long-term Microzide (hydrochlorothiazide) increase skin cancer risk, and how do I protect myself?
Hydrochlorothiazide makes skin more sensitive to sunlight. MedlinePlus warns it "may make your skin sensitive to sunlight and increase your risk of a certain types of skin cancer." StatPearls adds that the FDA has flagged a small increased risk of non-melanoma skin cancer — particularly squamous cell carcinoma — in White patients with high cumulative exposure (cumulative hydrochlorothiazide dose); for most people the blood-pressure benefit is judged to outweigh this risk, but sun protection and skin checks are sensible. Practical steps: use broad-spectrum sunscreen, cover up, limit midday sun and tanning beds, and have any new, changing, or non-healing skin spot checked. Do not stop the medication on your own over this concern — discuss your personal risk with your prescriber first.
When does Microzide (hydrochlorothiazide) start working and how long do side effects last?
The diuretic (urination) effect begins within about 2 hours of a dose and generally eases over the day, which is why many people take it in the morning to avoid nighttime bathroom trips. Blood-pressure lowering builds over days to a few weeks of regular use. Early dizziness and extra urination often settle as your body adjusts. The vision and electrolyte problems above can appear at any time — some, like acute myopia and angle-closure glaucoma, tend to strike within the first days (StatPearls). Do not stop hydrochlorothiazide on your own if you feel better or worse; stopping can let your blood pressure climb back up, so any change should be guided by your prescriber. This is not a complete list of side effects — check MedlinePlus or ask your pharmacist.
Cite this page
- APA
- pharmaranks. (2026, July 24). Hydrochlorothiazide: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/hydrochlorothiazide
- MLA
- “Hydrochlorothiazide: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/hydrochlorothiazide.
We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.
Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.
Read the full FDA label for hydrochlorothiazide on DailyMed (NIH) ↗.