NDC 68788-7475 Hydrochlorothiazide


NDC Product Code 68788-7475

NDC CODE: 68788-7475

Proprietary Name: Hydrochlorothiazide What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Hydrochlorothiazide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Hydrochlorothiazide belongs to a class of drugs known as diuretics/water pills. It works by causing you to make more urine. This helps your body get rid of extra salt and water. This medication also reduces extra fluid in the body (edema) caused by conditions such as heart failure, liver disease, or kidney disease. This can lessen symptoms such as shortness of breath or swelling in your ankles or feet.

Product Characteristics

BLUE (C48333)
Shape: CAPSULE (C48336)
15 MM
Score: 1

NDC Code Structure

NDC 68788-7475-1

Package Description: 100 CAPSULE in 1 BOTTLE

NDC 68788-7475-3

Package Description: 30 CAPSULE in 1 BOTTLE

NDC 68788-7475-6

Package Description: 60 CAPSULE in 1 BOTTLE

NDC 68788-7475-7

Package Description: 7 CAPSULE in 1 BOTTLE

NDC 68788-7475-9

Package Description: 90 CAPSULE in 1 BOTTLE

NDC Product Information

Hydrochlorothiazide with NDC 68788-7475 is a a human prescription drug product labeled by Preferred Pharmaceuticals Inc.. The generic name of Hydrochlorothiazide is hydrochlorothiazide. The product's dosage form is capsule and is administered via oral form.

Labeler Name: Preferred Pharmaceuticals Inc.

Dosage Form: Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.

Product Type: Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Hydrochlorothiazide Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C RED NO. 28 (UNII: 767IP0Y5NH)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • SHELLAC (UNII: 46N107B71O)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Increased Diuresis - [PE] (Physiologic Effect)
  • Thiazide Diuretic - [EPC] (Established Pharmacologic Class)
  • Thiazides - [CS]

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Preferred Pharmaceuticals Inc.
Labeler Code: 68788
FDA Application Number: ANDA078164 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 02-28-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Hydrochlorothiazide Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index


Hydrochloro‑thiazide is the 3,4-dihydro derivative of chlorothiazide. Its chemical name is 6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide. Its molecular formula is C7H8ClN3O4S2; its molecular weight is 297.74; and its structural formula is: It is a white, or practically white, crystalline powder which is slightly soluble in water, but freely soluble in sodium hydroxide solution.Hydrochloro‑thiazide is supplied as 12.5 mg capsules for oral use. Each capsule contains the following inactive ingredients: colloidal silicon dioxide, corn starch, lactose monohydrate, and magnesium stearate. The hard gelatin shell consists of gelatin, titanium dioxide, sodium lauryl sulphate, FD&C Blue #1, D&C Red #28, D&C Yellow #10, black iron oxide and shellac.

Clinical Pharmacology

Hydrochlorothiazide blocks the reabsorption of sodium and chloride ions, and it thereby increases the quantity of sodi‑um traversing the distal tubule and the volume of water excret‑ed. A portion of the additional sodium presented to the distal tubule is exchanged there for potassium and hydrogen ions. With continued use of hydro‑chlorothiazide and depletion of sodium, compensatory mecha‑nisms tend to increase this exchange and may produce excessive loss of potassium, hydrogen and chloride ions. Hydrochlorothiazide also decreases the excretion of cal‑cium and uric acid, may increase the excretion of iodide and may reduce glomerular fil‑tration rate. Metabolic toxicities associated with excessive elec‑trolyte changes caused by hydrochlorothiazide have been shown to be dose-related.

Pharmacokinetics And Metabolism

Hydrochlorothiazide is well absorbed (65% to 75%) fol‑lowing oral administration. Absorption of hydrochlorothi‑azide is reduced in patients with congestive heart failure.Peak plasma concentrations are observed within 1 to 5 hours of dosing, and range from 70 to 490 ng/mL follow‑ing oral doses of 12.5 to 100 mg. Plasma concentra‑tions are linearly related to the administered dose. Concen‑trations of hydrochlorothiazide are 1.6 to 1.8 times higher in whole blood than in plasma. Binding to serum proteins has been reported to be approxi‑mately 40% to 68%. The plas‑ma elimination half-life has been reported to be 6 to 15 hours. Hydrochlorothiazide is eliminated primarily by renal pathways. Following oral doses of 12.5 to 100 mg, 55% to 77% of the administered dose appears in urine and greater than 95% of the absorbed dose is excreted in urine as unchanged drug. In patients with renal disease, plasma con‑centrations of hydrochlorothi‑azide are increased and the elimination half-life is pro‑longed.When hydrochloro‑thiazide is adminis‑tered with food, its bioavailabil‑ity is reduced by 10%, the max‑imum plasma concentration is reduced by 20%, and the time to maximum concentration increases from 1.6 to 2.9 hours.


Acute antihypertensive effects of thi‑azides are thought to result from a reduction in blood vol‑ume and cardiac output, sec‑ondary to a natriuretic effect, although a direct vasodilatory mechanism has also been pro‑posed. With chronic adminis‑tration, plasma volume returns toward normal, but peripheral vascular resistance is de‑creased. The exact mechanism of the anti-hypertensive effect of hydrochlorothiazide is not known. Thiazides do not affect normal blood pressure. Onset of action occurs within 2 hours of dos‑ing, peak effect is observed at about 4 hours, and activity per‑sists for up to 24 hours.

Clinical Studies

In an 87 patient 4-week double-blind, placebo-controlled, parallel group trial, patients who received hydrochloro‑thiazide had reductions in seated systolic and diastolic blood pressure that were significantly greater than those seen in patients who received placebo. In published placebo-controlled trials com‑paring 12.5 mg of hydrochlorothiazide to 25 mg, the 12.5 mg dose preserved most of the placebo-corrected blood pressure reduction seen with 25 mg.

Indications And Usage

Hydrochloro‑thiazide capsules USP are indicated in the management of hypertension either as the sole therapeutic agent, or in combination with other antihypertensives. Unlike potassium sparing combina‑tion diuretic products, hydrochloro‑thiazide capsules USP may be used in those patients in whom the development of hyperkalemia cannot be risked, including patients taking ACE inhibitors.

Usage In Pregnancy

The rou‑tine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unneces‑sary hazard. Diuretics do not prevent development of tox‑emia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of developed toxemia.Edema during pregnancy may arise from pathological causes or from the physiologic and mechanical consequences of pregnancy. Diuretics are indi‑cated in pregnancy when edema is due to pathologic causes, just as they are in the absence of pregnancy. Dependent edema in pregnan‑cy resulting from restriction of venous return by the expanded uterus is properly treated through elevation of the lower extremities and use of support hose; use of diuretics to lower intravascular volume in this case is illogical and unneces‑sary. There is hypervolemia during normal pregnancy which is harmful to neither the fetus nor the mother (in the absence of cardiovascular dis‑ease), but which is associated with edema, including general‑ized edema in the majority of pregnant women. If this edema produces discomfort, in‑creased recumbency will often provide relief. In rare instances this edema may cause extreme discomfort which is not relieved by rest. In these cases a short course of diuretics may provide relief and may be appropriate.


Hydrochlorothiazide capsules are con‑traindicated in patients with anuria. Hypersensitivity to this product or other sulfonamide derived drugs is also con‑traindicated.


Diabetes and Hypoglycemia: Latent diabetes mellitus may become manifest and diabetic patients given thiazides may require adjustment of their insulin dose. Renal Disease: Cumulative effects of the thiazides may develop in patients with impaired renal function. In such patients, thiazides may precipitate azotemia.


Electrolyte and Fluid Balance Status: In published studies, clinically significant hypokalemia has been consistently less common in patients who received 12.5 mg of hydro‑chlorothiazide than in patients who received higher doses. Nevertheless, periodic determi‑nation of serum electrolytes should be performed in patients who may be at risk for the development of hypo‑kalemia. Patients should be observed for signs of fluid or electrolyte disturbances, i.e., hyponatremia, hypochloremic alkalosis, and hypokalemia and hypomagnesemia.Warning signs or symptoms of fluid and electrolyte imbalance include dryness of mouth, thirst, weakness, lethargy, drowsiness, restlessness, muscle pains or cramps, mus‑cular fatigue, hypotension, oliguria, tachycardia, and gas‑trointestinal disturbances such as nausea and vomiting.Hypokalemia may develop, especially with brisk diuresis when severe cirrhosis is pres‑ent, during concomitant use of corticosteroid or adrenocorti‑cotropic hormone (ACTH) or after prolonged therapy. Interference with adequate oral electrolyte intake will also con‑tribute to hypokalemia. Hypo‑kalemia and hypomagnesemia can provoke ventricular arrhythmias or sensitize or exaggerate the response of the heart to the toxic effects of dig‑italis. Hypokalemia may be avoided or treated by potas‑sium supplementation or increased intake of potassium rich foods.Dilutional hyponatremia is life-threatening and may occur in edematous patients in hot weather; appropriate therapy is water restriction rather than salt administration, except in rare instances when the hypo‑natremia is life-threatening. In actual salt depletion, appropri‑ate replacement is the therapy of choice.Hyperuricemia: Hyperuricemia or acute gout may be precipi‑tated in certain patients receiv‑ing thiazide diuretics.Impaired Hepatic Function: Thiazides should be used with caution in patients with impaired hepatic function. They can precipitate hepatic coma in patients with severe liver dis‑ease. Parathyroid Disease: Calcium excretion is decreased by thi‑azides, and pathologic changes in the parathyroid glands, with hypercalcemia and hypophos‑phatemia, have been observed in a few patients on prolonged thiazide therapy.

Drug Interactions

When given concurrently the following drugs may interact with thiazide diuretics: Alcohol, barbiturates, or narcotics - potentiation of ortho‑static 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 re‑duce its absorption from the gastrointestinal tract by up to 85 and 43 percent, respectively.Corticosteroid, ACTH - intensi‑fied 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, non-depolarizing (e.g., tubocurarine) - possible increased responsiveness to the muscle relaxant. Lithium - generally should not be given with diuretics. Diuretic agents reduce the renal clear‑ance of lithium and greatly increase the risk of lithium tox‑icity. Refer to the package insert for lithium preparations before use of such preparations with hydrochloro‑thiazide.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 hydrochloro‑thiazide 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 hepato-carcinogenicity in male mice.  Hydrochlorothiazide was not genotoxic in vitro in the Ames mutagenicity assay of Salmonella typhimurium strains TA 98, TA100, 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 1300 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.

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.

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.

Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

Geriatric Use

A greater blood pressure reduction and an increase in side effects may be observed in the elderly (i.e., >65 years) with hydrochlorothiazide. Starting treatment with the lowest available dose of hydrochlorothiazide (12.5 mg) is therefore recommended. If further titration is required, 12.5 mg increments should be utilized.

Adverse Reactions

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 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.


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 LD50 of hydrochlorothiazide is greater than 10 g/kg in the mouse and rat.

Dosage And Administration

For Control of Hypertension: The adult initial dose of hydrochloro‑thiazide 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.

How Supplied

Hydrochlorothiazide Capsules USP 12.5 mg are blue/blue size ‘4’ hard gelatin capsules, imprinted with ‘D’ on blue cap and ‘26’ on blue body with black edible ink, filled with white to off-white powder.Bottles of 7               NDC 68788-7475-7Bottles of 30               NDC 68788-7475-3Bottles of 60               NDC 68788-7475-6Bottles of 90               NDC 68788-7475-9Bottles of 100               NDC 68788-7475-1 Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30° C (59° to 86°F) [ see USP Controlled Room Temperature]. Protect from light, moisture, freezing, -20°C  (-4°F).Distributed by: Rising Health, LLC Saddle Brook, NJ 07663Made in India Code: TS/DRUGS/19/1993 Revised: 01/201Repackaged By: Preferred Pharmaceuticals Inc.

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