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Hydrochlorothiazide 50 mg Tablet, 1,000-count — NDC 29300-0129-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Hydrochlorothiazide 50 mg Tablet, 1,000-count — NDC 29300-129-10 (Billing 29300-0129-10)

by Unichem Pharmaceuticals (USA), Inc. · 1000 TABLET in 1 BOTTLE

This is a package of 1,000 tablets of Hydrochlorothiazide 50 mg Tablet from Unichem Pharmaceuticals (USA), Inc., marketed since Aug 2008 and currently FDA-listed; retail pharmacies pay about $0.0317 per tablet (NADAC). It is the main listing for this product, which comes in 4 package sizes.

NDC 29300-0129-10
🏷️ FDA NDC (as labeled) 29300-129-10 billing pads the product segment with a zero
This package
Contains1,000-count Cost per ea$0.0317 NADAC Per package$31.70 / 1000 tablets Pack sizes4 compare ↓
Also priced by: Medicaid pays $0.1546/unit · Part D plans $0.0822/unit — full pricing hub ↓
Main listing for product 29300-129 · Also comes in: 100 tablets 29300-129-01 500 tablets 29300-129-05 5000 tablets 29300-129-50
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

NDC database record

One package, one record: these facts belong to NDC 29300-129-10 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
29300 labeler · 129 product · 10 package
Package marketed since
Jul 2, 2009
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Billing quantity
1,000 EA per package
Barcode (UPC)
0329300129014, 0329300128017
Medicaid fills, this package
39,191 prescriptions in the last four reported quarters
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 29300-129-10
Product NDC 29300-129
11-digit billing NDC 29300012910
NCPDP billing unit EA — each (per item)
RxCUI 197770, 310798, 429503
UNII 0J48LPH2TH
UPC 0329300129014, 0329300128017
Application # ANDA040907
SPL Set ID 33f3b980-b339-4dbf-99bd-05588c2a298c
Established class (EPC) Thiazide Diuretic
Physiologic effect Increased Diuresis
Chemical class Thiazides
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-08-15
Route ORAL
Dosage form TABLET
Substance HYDROCHLOROTHIAZIDE
TE code (Orange Book) AB · RLD · RS

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 37600040000310
GPI class hydroCHLOROthiazide
GCN Seq No 008183
GCN 34825
HICL code 003649
Ingredient (HICL) Hydrochlorothiazide
HIC1 code R
Therapeutic class — broad (HIC1) Kidney/Urinary Tract
HIC2 code R1
Therapeutic class — intermediate (HIC2) Affect Primarily Kidneys/Urinary Tract
HIC3 code R1F
Therapeutic class — specific (HIC3) Thiazide And Related Diuretics
AHFS code 24:36.20.00
AHFS class Thiazide Diuretics (24:36)
FDB label name HYDROCHLOROTHIAZIDE 50 MG TAB
FDB brand name Hydrochlorothiazide
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 008183
  • GCN: 34825
  • GPI-14 (Medi-Span): 37600040000310
  • HICL (First Databank): 003649
  • AHFS class code: 24:36.20.00
  • RxCUI (RxNorm): 197770
Why two NDCs? The FDA registers this code as 29300-129-10 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 29300-0129-10. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Thiazide Diuretic class.

Pharmacologic class Thiazide Diuretic
Drug family (ATC) Renin-inhibitors, Thiazides, plain
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

Label name HYDROCHLOROTHIAZIDE 50 MG TAB Ingredient Hydrochlorothiazide
📖 What it is MedlinePlus · NLM

Hydrochlorothiazide is used alone or in combination with other medications to treat high blood pressure. Hydrochlorothiazide is used to treat edema (fluid retention; excess fluid held in body tissues) caused by various medical problems, including heart, kidney, and liver disease and to treat edema caused by using certain medications including estrogen and corticosteroids. Hydrochlorothiazide is in a class of medications called diuretics ('water pills'). It works by causing the kidneys to get rid of unneeded water and salt from the body into the urine. High blood pressure is a common condition...

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It lowers high blood pressure, which helps reduce the risk of strokes and heart attacks. Some products, such as Inzirqo and the tablets, are also used for swelling from conditions...
  • Take it by mouth exactly as prescribed, usually once a day. For swelling, your prescriber may have you take it only some days of the week. Food slightly lowers absorption, so ask m...
  • Dizziness, lightheadedness when standing, stomach upset, headache and weakness are the usual ones. Stand up slowly, and be careful with alcohol since it can worsen dizziness. Use s...
  • Call for eye pain or sudden vision changes, severe rash or blistering, trouble breathing, severe stomach pain, yellow skin or eyes, or unusual bruising or infections. Also call for...
📖 Read our full Hydrochlorothiazide guide →
8
Nutrient depletion considerations

Hydrochlorothiazide may be associated with lower levels of 8 nutrients — worth a chat with your pharmacist, not a cause for alarm.

An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eaPer package
Retail pharmacies payNADAC · weekly $0.032 $31.70 / 1000 tablets
Medicaid paysCMS SDUD · 12 mo $0.1546 $154.60 / 1000 tablets
Medicare drug plans payPart D · Q2 2026 $0.0822 $82.20 / 1000 tablets
NADAC price history (per ea) — tap or hover for the price & month
Jan 2022 Aug 2022 Jan 2026 Sep 2026 $0.039 $0.024
▲ Up 14% over the last 24 months.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Per unit Per pack Marketing startMarketing endStatus
29300-0129-01 29300-129-01 100 TABLET in 1 BOTTLE $0.0317 / ea $3.17 2009-07-02 — Active
29300-0129-05 29300-129-05 500 TABLET in 1 BOTTLE — — 2009-07-02 — Active
29300-0129-10 You're viewing this Main listing 1000 TABLET in 1 BOTTLE $0.0317 / ea $31.65 2009-07-02 — Active
29300-0129-50 29300-129-50 5000 TABLET in 1 BOTTLE — — 2009-07-02 — Active

You're viewing one of 4 pack sizes for this product.

This pack effectively ties for the lowest per-ea cost of the 2 priced pack sizes ($0.0317 NADAC).

In Medicaid, this is the most-dispensed pack of this product — about 75% of fills over the last four reported quarters. See all packs ↓

Pack size FAQ

What quantity is in this package?
This is a 1,000-count package — 1000 tablet in 1 bottle.
How does this package differ from NDC 29300-0129-01?
Both are Hydrochlorothiazide 50 mg Tablet — the drug itself is identical. This page's package is the 1,000-count one, while NDC 29300-0129-01 is the 100 tablets package.
What NDC number is used to bill for this package of Hydrochlorothiazide 50 mg Tablet?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Hydrochlorothiazide 50 mg 00172-2089-60 Teva 100 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 16729-0184-01 Accord 100 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 23155-0009-01 Heritage 100 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mgthis 29300-0129-10 Unichem 1000 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 62135-0449-05 Chartwell 500 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 65862-0134-01 Aurobindo 100 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 69315-0130-01 Leading 100 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 69584-0362-10 Oxford 100 tablets $0.032 AB Availability likely —
Hydrochlorothiazide 50 mg 43063-0747-01 PD-Rx 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 43353-0240-45 Aphena 45 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 43353-0717-09 Aphena 9000 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 43547-0398-01 Solco 10 tablets — — FDA listed —
Hydrochlorothiazide 50 mg 50090-6156-00 A-S 30 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 50090-6532-00 A-S 30 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 50228-0112-10 ScieGen 1000 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 51407-0332-01 Golden 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 51655-0422-26 Northwind 90 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 51655-0506-26 Northwind 90 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 63187-0441-30 Proficient 30 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 63629-1220-01 Bryant 100 tablets — — FDA listed —
Hydrochlorothiazide 50 mg 63629-8992-01 Bryant 30 tablets — — FDA listed —
Hydrochlorothiazide 50 mg 68071-2405-01 NuCare 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 68071-3323-03 NuCare 30 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 68788-7790-00 Preferred 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 70518-3780-00 REMEDYREPACK 90 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 70518-4525-00 REMEDYREPACK 90 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 71205-0090-00 Proficient 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 71205-0751-30 Proficient 30 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 71335-0145-00 Bryant 45 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 71335-1451-00 Bryant 45 tablets — — FDA listed —
Hydrochlorothiazide 50 mg 71335-1976-00 Bryant 45 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 71610-0471-45 Aphena 45 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 72162-1357-01 Bryant 100 tablets — — FDA listed —
Hydrochlorothiazide 50 mg 72189-0263-90 DIRECT 90 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 72189-0513-90 Direct_Rx 90 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 72789-0303-01 PD-Rx 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 76282-0155-01 Exelan 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 82804-0031-30 Proficient 30 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 82804-0973-00 Proficient 100 tablets — AB FDA listed —
Hydrochlorothiazide 50 mg 82868-0016-90 Northwind 90 tablets — AB FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2008
On the market since
Aug 2008
📍
2026
Currently FDA-listed
18 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color Orange
ShapeRound
ImprintH1;U
Size6 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

🧪 Avoiding an ingredient? See Hydrochlorothiazide inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerUnichem Pharmaceuticals (USA), Inc.
Application holderUNICHEM LABORATORIES LTD
FDA applicationANDA040907 (ANDA)
Labeler code29300
First marketedAug 2008
Product typeHuman Prescription Drug
Portfolio210 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Very long sections are excerpted here and marked; the full text is on DailyMed (linked in the sources below). Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ~1 min read ▾

INDICATIONS AND USAGE Hydrochlorothiazide tablets are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Hydrochlorothiazide tablets have also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. Hydrochlorothiazide tablets are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension.

Use in Pregnancy Routine use of diuretics during normal pregnancy is inappropriate and exposes mother and fetus to unnecessary hazard. Diuretics do not prevent development of toxemia of pregnancy and there is no satisfactory evidence that they are useful in the treatment of toxemia. Edema during pregnancy may arise from pathologic causes or from the physiologic and mechanical consequences of pregnancy.

Thiazides are indicated in pregnancy when edema is due to pathologic causes, just as they are in the absence of pregnancy (see PRECAUTIONS: Pregnancy ). Dependent edema in pregnancy, resulting from restriction of venous return by the gravid uterus, is properly treated through elevation of the lower extremities and use of support stockings. Use of diuretics to lower intravascular volume in this instance is illogical and unnecessary.

During normal pregnancy there is hypervolemia which is not harmful to the fetus or the mother in the absence of cardiovascular disease. However, it may be associated with edema, rarely generalized edema. If such edema causes discomfort, increased recumbency will often provide relief.

Rarely this edema may cause extreme discomfort which is not relieved by rest. In these instances, a short course of diuretic therapy may provide relief and be appropriate.

⏱️ Dosage and Administration ~1 min read ▾

DOSAGE AND ADMINISTRATION Therapy should be individualized according to patient response. Use the smallest dosage necessary to achieve the required response. Adults For Edema The usual adult dosage is 25 mg to 100 mg daily as a single or divided dose.

Many patients with edema respond to intermittent therapy, i.e., administration on alternate days or on 3 to 5 days each week. With an intermittent schedule, excessive response and the resulting undesirable electrolyte imbalance are less likely to occur. For Control of Hypertension The usual initial dose in adults is 25 mg daily given as a single dose.

The dose may be increased to 50 mg daily, given as a single or two divided doses. Doses above 50 mg are often associated with marked reductions in serum potassium (see also PRECAUTIONS ). Patients usually do not require doses in excess of 50 mg of hydrochlorothiazide daily when used concomitantly with other antihypertensive agents.

Infants and Children For Diuresis and for Control of Hypertension The usual pediatric dosage is 0.5 mg to 1 mg per pound (1 to 2 mg/kg) per day in single or two divided doses, not to exceed 37.5 mg per day in infants up to 2 years of age or 100 mg per day in children 2 to 12 years of age. In infants less than 6 months of age, doses up to 1.5 mg per pound (3 mg/kg) per day in two divided doses may be required. (See PRECAUTIONS: Pediatric Use .)

⛔ Contraindications 11 words ▾

CONTRAINDICATIONS Anuria. Hypersensitivity to this product or to other sulfonamide-derived drugs.

⚠️ Warnings 209 words ▾

WARNINGS Use with caution in severe renal disease. In patients with renal disease, thiazides may precipitate azotemia. Cumulative effects of the drug may develop in patients with impaired renal function.

Thiazides should be used with caution in patients with impaired hepatic function or progressive liver disease, since minor alterations of fluid and electrolyte balance may precipitate hepatic coma. Thiazides may add to or potentiate the action of other antihypertensive drugs. Sensitivity reactions may occur in patients with or without a history of allergy or bronchial asthma.

The possibility of exacerbation or activation of systemic lupus erythematosus has been reported. Lithium generally should not be given with diuretics (see PRECAUTIONS, Drug Interactions ). Acute Myopia and Secondary Angle-Closure Glaucoma Hydrochlorothiazide, a sulfonamide, can cause an idiosyncratic reaction, resulting in acute transient myopia and acute angle-closure glaucoma.

Symptoms include acute onset of decreased visual acuity or ocular pain and typically occur within hours to weeks of drug initiation. Untreated acute angle-closure glaucoma can lead to permanent vision loss. The primary treatment is to discontinue hydrochlorothiazide as rapidly as possible.

Prompt medical or surgical treatments may need to be considered if the intraocular pressure remains uncontrolled. Risk factors for developing acute angle-closure glaucoma may include a history of sulfonamide or penicillin allergy.

🤒 Adverse Reactions ~1 min read ▾

ADVERSE REACTIONS The following adverse reactions have been reported and, within each category, are listed in 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, paresthesias, dizziness, headache, restlessness.

Renal: Renal failure, renal dysfunction, interstitial nephritis (see WARNINGS ). Skin: Erythema multiforme including Stevens-Johnson Syndrome, exfoliative dermatitis including toxic epidermal necrolysis, alopecia. Special Senses: Transient blurred vision, xanthopsia.

Urogenital: Impotence. Whenever adverse reactions are moderate or severe, thiazide dosage should be reduced or therapy withdrawn. Postmarketing Experience: Non-melanoma Skin Cancer Hydrochlorothiazide is associated with an increased risk of non-melanoma skin cancer.

In a study conducted in the Sentinel System, increased risk was predominantly for squamous cell carcinoma (SCC) and in white patients taking large cumulative doses. The increased risk for SCC in the overall population was approximately 1 additional case per 16,000 patients per year, and for white patients taking a cumulative dose of ≥ 50,000 mg the risk increase was approximately 1 additional SCC case for every 6,700 patients per year.

🔄 Drug Interactions 218 words ▾

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 Absorption of hydrochlorothiazide is impaired in the presence of anionic exchange resins. Single doses of either cholestyramine or colestipol resins bind the hydrochlorothiazide and reduce its absorption from the gastrointestinal tract by up to 85 and 43 percent, respectively.

Corticosteroids, 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 add a high 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. Therefore, when hydrochlorothiazide and non-steroidal anti-inflammatory agents are used concomitantly, the patient should be observed closely to determine if the desired effect of the diuretic is obtained.

🤰 Pregnancy 107 words ▾

Pregnancy Teratogenic Effects-Pregnancy Category B Studies in which hydrochlorothiazide was orally administered to pregnant mice and rats during their respective periods of major organogenesis at doses up to 3000 and 1000 mg hydrochlorothiazide/kg, respectively, provided no evidence of harm to the fetus. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Nonteratogenic Effects Thiazides cross the placental barrier and appear in cord blood. There is a risk of fetal or neonatal jaundice, thrombocytopenia, and possibly other adverse reactions that have occurred in adults.

🧒 Pediatric Use 48 words ▾

Pediatric Use There are no well controlled clinical trials in pediatric patients. Information on dosing in this age group is supported by evidence from empiric use in pediatric patients and published literature regarding the treatment of hypertension in such patients. (See DOSAGE AND ADMINISTRATION: Infants and Children .)

🆘 Overdosage 104 words ▾

OVERDOSAGE The most common signs and symptoms observed are those caused by electrolyte depletion (hypokalemia, hypochloremia, hyponatremia) and dehydration resulting from excessive diuresis. If digitalis has also been administered, hypokalemia may accentuate cardiac arrhythmias. In the event of overdosage, symptomatic and supportive measures should be employed.

Emesis should be induced or gastric lavage performed. Correct dehydration, electrolyte imbalance, hepatic coma and hypotension by established procedures. If required, give oxygen or artificial respiration for respiratory impairment.

The degree to which hydrochlorothiazide is removed by hemodialysis has not been established. The oral LD 50 of hydrochlorothiazide is greater than 10 g/kg in the mouse and rat.

🧬 Clinical Pharmacology 152 words ▾

CLINICAL PHARMACOLOGY The mechanism of the antihypertensive effect of thiazides is unknown. Hydrochlorothiazide does not usually affect normal blood pressure. Hydrochlorothiazide affects the distal renal tubular mechanism of electrolyte reabsorption.

At maximal therapeutic dosage all thiazides are approximately equal in their diuretic efficacy. Hydrochlorothiazide increases excretion of sodium and chloride in approximately equivalent amounts. Natriuresis may be accompanied by some loss of potassium and bicarbonate.

After oral use diuresis begins within 2 hours, peaks in about 4 hours and lasts about 6 to 12 hours. Pharmacokinetics and Metabolism Hydrochlorothiazide is not metabolized but is eliminated rapidly by the kidney. 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.

At least 61 percent of the oral dose is eliminated unchanged within 24 hours. Hydrochlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.

📦 How Supplied / Storage and Handling ~1 min read ▾

HOW SUPPLIED Hydrochlorothiazide Tablets, USP are available as light orange, mottled, circular, flat, beveled, uncoated tablets, debossed with "H1" on one side and "U" on other side containing 12.5 mg of hydrochlorothiazide, USP. Bottles of 100 : NDC 29300-485-01 Bottles of 1,000 : NDC 29300-485-10 Hydrochlorothiazide Tablets, USP are available as light orange, circular, flat, beveled, uncoated tablets, with score line having "U" and "128" debossed across the score line on one side and plain on other side containing 25 mg of hydrochlorothiazide, USP.

Bottles of 100 : NDC 29300-128-01 Bottles of 500 : NDC 29300-128-05 Bottles of 1,000 : NDC 29300-128-10 Bottles of 5,000 : NDC 29300-128-50 Hydrochlorothiazide Tablets, USP are available as light orange, circular, flat, beveled, uncoated tablets, with score line having "U" and "129" debossed across the score line on one side and plain on other side containing 50 mg of hydrochlorothiazide, USP. Bottles of 100 : NDC 29300-129-01 Bottles of 500 : NDC 29300-129-05 Bottles of 1,000 : NDC 29300-129-10 Bottles of 5,000 : NDC 29300-129-50 PHARMACIST: Dispense in a well-closed container as defined in the USP.

Use child-resistant closure (as required) Store at 20° to 25° C (68° to 77° F) [see USP Controlled Room Temperature]. KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN. Please address medical inquiries to Unichem's toll free # 1-866-562-4616.

Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Manufactured for: East Brunswick, NJ 08816 09-R-05/2025 13014161 Company Logo

📋 Description 120 words ▾

DESCRIPTION Hydrochlorothiazide, USP is a diuretic and antihypertensive. It is the 3, 4-dihydro derivative of chlorothiazide. It is chemically designated as 6-chloro-3, 4-dihydro-2 H -1, 2, 4- benzothiadiazine-7-sulfonamide 1, 1-dioxide and has the following structural formula: Hydrochlorothiazide, USP is a white, or practically white, crystalline powder which is slightly soluble in water, freely soluble in sodium hydroxide solution, in n-butylamine, and in dimethylformamide; sparingly soluble in methanol; insoluble in ether, in chloroform, and in dilute mineral acids.

Each tablet for oral administration contains 12.5 mg, 25 mg or 50 mg hydrochlorothiazide, USP. In addition, each tablet contains the following inactive ingredients: corn starch, FD&C Yellow #6, dibasic calcium phosphate, pregelatinized starch, colloidal silicon dioxide, lactose monohydrate and magnesium stearate. Hydrochlorothiazide

💬 Information for Patients 22 words ▾

Information for Patients Non-melanoma Skin Cancer: Instruct patients taking hydrochlorothiazide to protect skin from the sun and undergo regular skin cancer screening.

⚠️ Precautions ~2 min read ▾

PRECAUTIONS General All patients receiving diuretic therapy should be observed for evidence of fluid or electrolyte imbalance: namely, hyponatremia, hypochloremic alkalosis, and hypokalemia. Serum and urine electrolyte determinations are particularly important when the patient is vomiting excessively or receiving parenteral fluids. Warning signs or symptoms of fluid and electrolyte imbalance, irrespective of cause, include dryness of mouth, thirst, weakness, lethargy, drowsiness, restlessness, confusion, seizures, muscle pains or cramps, muscular fatigue, hypotension, oliguria, tachycardia, and gastrointestinal disturbances such as nausea and vomiting.

Hypokalemia may develop, especially with brisk diuresis, when severe cirrhosis is present or after prolonged therapy. Interference with adequate oral electrolyte intake will also contribute to hypokalemia. Hypokalemia may cause cardiac arrhythmia and may also sensitize or exaggerate the response of the heart to the toxic effects of digitalis (e.g., increased ventricular irritability).

Hypokalemia may be avoided or treated by use of potassium sparing diuretics or potassium supplements such as foods with a high potassium content. Although any chloride deficit is generally mild and usually does not require specific treatment except under extraordinary circumstances (as in liver disease or renal disease), chloride replacement may be required in the treatment of metabolic alkalosis. Dilutional hyponatremia may occur in edematous patients in hot weather; appropriate therapy is water restriction, rather than administration of salt, except in rare instances when the hyponatremia is life threatening.

In actual salt depletion, appropriate replacement is the therapy of choice. Hyperuricemia may occur or acute gout may be precipitated in certain patients receiving thiazides. In diabetic patients dosage adjustments of insulin or oral hypoglycemic agents may be required.

Hyperglycemia may occur with thiazide diuretics. Thus latent diabetes mellitus may become manifest during thiazide therapy. The antihypertensive effects of the drug may be enhanced in the post-sympathectomy patient.

If progressive renal impairment becomes evident, consider withholding or discontinuing diuretic therapy. Thiazides have been shown to increase the urinary excretion of magnesium; this may result in hypomagnesemia. Thiazides may decrease urinary calcium excretion.

Thiazides may cause intermittent and slight elevation of serum calcium in the absence of known disorders of calcium metabolism. Marked hypercalcemia may be evidence of hidden hyperparathyroidism. Thiazides should be discontinued before carrying out tests for parathyroid function.

Increases in cholesterol and triglyceride levels may be associated with thiazide diuretic therapy. Information for Patients Non-melanoma Skin Cancer: Instruct patients taking hydrochlorothiazide to protect skin from the sun and undergo regular skin cancer screening. Laboratory Tests Periodic determination of serum electrolytes to detect possible electrolyte imbalance should be done at appropriate intervals.

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 Absorption of hydrochlorothiazide is impaired in the presence of anionic exchange resins. Single doses of either cholestyramine or colestipol resins bind the hydrochlorothiazide and reduce its absorption from the gastrointestinal tract by up to 85 and 43 percent, respectively.

Corticosteroids, 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 mu… [Excerpted — this section continues on DailyMed.]

🍼 Nursing Mothers 43 words ▾

Nursing Mothers Thiazides are excreted in breast milk. Because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue nursing or to discontinue hydrochlorothiazide, taking into account the importance of the drug to the mother.

📄 Package Label / Principal Display Panel 24 words ▾

PRINCIPAL DISPLAY PANEL Hydrochlorothiazide Tablets USP 12.5 mg Hydrochlorothiazide Tablets USP 25 mg Hydrochlorothiazide Tablets USP 50 mg Container Label Container Label Container Label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicaid utilization & spend

📍 This exact package only: Medicaid data is reported per full 11-digit NDC — labeler, product and pack size — so every number here is for this package alone, not the drug overall. Other pack sizes report separately.
💊 Pharmacy benefit only: These are Medicaid outpatient pharmacy claims, billed by NDC. They exclude the medical benefit — clinic- or hospital-administered drugs billed under HCPCS J-codes — so drugs used mostly that way (e.g. Avastin, Lucentis, Keytruda) can look low or missing here. That’s expected, not an error.
📅 Q1 2025 – Q1 2026 · 5 quarters of data
ⓘ The newest quarter is usually incomplete when first published; states restate recent quarters in later CMS releases, so the latest figures typically revise upward. State coverage-policy changes can also shift quarter-to-quarter totals.
Prescriptions last 4 qtrs
39.2K
Units reimbursed last 4 qtrs
2M
Gross reimbursed last 4 qtrs
$311.8K
Avg / prescription
$7.96
Avg / unit
$0.1546
Latest quarter Q1 2026
8.8KRx
Medicaid pays / ea
$0.1546
gross reimbursed
vs
NADAC / ea
$0.0317
acquisition cost
=
Spread
+$0.1229
+388% vs cost
What Medicaid paid per ea (before rebates; includes the pharmacy’s dispensing fee) compared with NADAC — the average price pharmacies pay to buy the drug. A positive spread means Medicaid reimbursed more than the purchase price, before manufacturer rebates.
Fee-for-service vs managed care ⓘ
37% FFS 63% MCO
Fee-for-service · 14,656 Rx Managed care · 24,535 Rx
State Medicaid map
Alaska: no data reported AK Maine: 11,896 units · 853 per 100k residents ME Washington: 38,264 units · 490 per 100k residents WA Idaho: 11,596 units · 590 per 100k residents ID Montana: 4,166 units · 368 per 100k residents MT North Dakota: 6,104 units · 780 per 100k residents ND Minnesota: 42,489 units · 741 per 100k residents MN Wisconsin: 54,673 units · 925 per 100k residents WI Michigan: 96,150 units · 958 per 100k residents MI New York: 201,981 units · 1,032 per 100k residents NY Vermont: 810 units · 125 per 100k residents VT New Hampshire: 5,193 units · 370 per 100k residents NH Oregon: 24,218 units · 572 per 100k residents OR Nevada: 18,124 units · 567 per 100k residents NV Wyoming: no data reported WY South Dakota: 1,230 units · 134 per 100k residents SD Iowa: 16,079 units · 501 per 100k residents IA Illinois: 165,777 units · 1,321 per 100k residents IL Indiana: 98,467 units · 1,435 per 100k residents IN Ohio: 136,969 units · 1,162 per 100k residents OH Pennsylvania: 130,372 units · 1,006 per 100k residents PA New Jersey: 61,512 units · 662 per 100k residents NJ Massachusetts: 23,329 units · 333 per 100k residents MA California: 185,857 units · 477 per 100k residents CA Utah: 1,650 units · 48.3 per 100k residents UT Colorado: 13,540 units · 230 per 100k residents CO Nebraska: 5,785 units · 292 per 100k residents NE Missouri: 55,942 units · 903 per 100k residents MO Kentucky: 59,671 units · 1,318 per 100k residents KY West Virginia: 37,704 units · 2,130 per 100k residents WV Virginia: 29,052 units · 333 per 100k residents VA Maryland: 56,459 units · 914 per 100k residents MD Connecticut: 25,797 units · 713 per 100k residents CT Rhode Island: 6,600 units · 603 per 100k residents RI Arizona: 13,529 units · 182 per 100k residents AZ New Mexico: 15,267 units · 722 per 100k residents NM Kansas: 5,385 units · 183 per 100k residents KS Arkansas: 15,171 units · 495 per 100k residents AR Tennessee: 33,526 units · 470 per 100k residents TN North Carolina: 51,766 units · 478 per 100k residents NC South Carolina: 3,216 units · 59.9 per 100k residents SC Delaware: 17,109 units · 1,659 per 100k residents DE Oklahoma: 24,973 units · 616 per 100k residents OK Louisiana: 24,390 units · 533 per 100k residents LA Mississippi: 5,574 units · 190 per 100k residents MS Alabama: 10,713 units · 210 per 100k residents AL Georgia: 8,320 units · 75.4 per 100k residents GA D.C.: 8,145 units · 1,200 per 100k residents DC Hawaii: no data reported HI Texas: 38,780 units · 127 per 100k residents TX Florida: 47,357 units · 209 per 100k residents FL
Units reimbursed · per 100k residents
48.32,130
gray = no data reported ⓘ
Colors are per 100,000 residents, so big states don’t automatically dominate. Tap or hover a state for its actual totals.
Tap or hover a state
…for its Medicaid breakdown
🏆 Top states by units · per 100k residents
1 West Virginia 2,130 /100k
2 Delaware 1,659 /100k
3 Indiana 1,435 /100k
4 Illinois 1,321 /100k
5 Kentucky 1,318 /100k
6 D.C. 1,200 /100k
7 Ohio 1,162 /100k
8 New York 1,032 /100k
National units — by quarter
💵 About the dollar figures: “reimbursed” is what Medicaid paid pharmacies before confidential manufacturer rebates, so the program’s real net cost is lower than these numbers. Fee-for-service and managed-care claims are combined unless split above. Source: CMS State Drug Utilization Data; per-100k rates use 2023 Census population estimates.

Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
1000 tablets this page29300-0129-10 39,191 Rx · $311,785
100 tablets29300-0129-01 13,215 Rx · $108,505
500 tablets29300-0129-05 No Medicaid data
5000 tablets29300-0129-50 No Medicaid data
Drug total (last 4 qtrs): 52,406 Rx · 2,565,591 units · $420,290 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Hydrochlorothiazide — the program that covers self-administered drugs. 17 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Hydrochlorothiazide. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$20.24M
Claims incl. refills
4.4M
Beneficiaries
3.6M
Spend / beneficiary
$5.65
Spend / claim
$4.63
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.