CHLORTHALIDONE tablet

Χώρα: Ηνωμένες Πολιτείες

Γλώσσα: Αγγλικά

Πηγή: NLM (National Library of Medicine)

Δραστική ουσία:

CHLORTHALIDONE (UNII: Q0MQD1073Q) (CHLORTHALIDONE - UNII:Q0MQD1073Q)

Διαθέσιμο από:

REMEDYREPACK INC.

Οδός χορήγησης:

ORAL

Τρόπος διάθεσης:

PRESCRIPTION DRUG

Θεραπευτικές ενδείξεις:

Diuretics such as chlorthalidone are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension. Chlorthalidone is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Chlorthalidone has also been found useful in edema due to various forms of renal dysfunction, such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. The routine use of diuretics in an otherwise healthy woman 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 developed toxemia. Edema during pregnancy may arise from pathologic causes or from the physiologic and mechanical consequences of pregnancy. Chlorthalidone is indicated in pregnancy when edema is due to

Περίληψη προϊόντος:

Chlorthalidone Tablets, USP are available containing 25 mg or 50 mg of chlorthalidone, USP. The 25 mg tablets are light yellow, round, unscored tablets debossed with M35 on one side of the tablet and blank on the other side. They are available as follows: NDC 0378-0222-77 bottles of 90 tablets NDC 0378-0222-01 bottles of 100 tablets NDC 0378-0222-10 bottles of 1000 tablets The 50 mg tablets are light green, round, scored tablets debossed with M to the left of the score and 75 to the right of the score on one side of the tablet and blank on the other side. They are available as follows: NDC 0378-0213-77 bottles of 90 tablets NDC 0378-0213-01 bottles of 100 tablets NDC 0378-0213-10 bottles of 1000 tablets Store at 20° to 25°C (68° to 77°F). [See USP for Controlled Room Temperature.] Protect from light. Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure.

Καθεστώς αδειοδότησης:

Abbreviated New Drug Application

Αρχείο Π.Χ.Π.

CHLORTHALIDONE- CHLORTHALIDONE TABLET
REMEDYREPACK INC.
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DESCRIPTION
Chlorthalidone an oral antihypertensive/diuretic. It is a monosulfamyl
diuretic that differs chemically
from thiazide diuretics in that a double-ring system is incorporated
in its structure. It is 2-Chloro-5(1-
hydroxy-3-oxo-1- isoindolinyl) benzenesulfonamide with the following
structural formula:
Chlorthalidone, USP is practically insoluble in water, in ether, and
in chloroform; soluble in methanol;
slightly soluble in ethanol.
Chlorthalidone tablets are available containing either 25 mg or 50 mg
of chlorthalidone, USP and the
following inactive ingredients: colloidal silicon dioxide, D&C Yellow
No.10 Aluminum Lake,
microcrystalline cellulose, pregelatinized starch (corn), sodium
starch glycolate (potato), stearic acid.
The 50 mg tablets also contain FD&C Blue No.1 Aluminum Lake.
CLINICAL PHARMACOLOGY
Chlorthalidone is an oral diuretic with prolonged action (48-72 hours)
and low toxicity. The major
portion of the drug is excreted unchanged by the kidneys. The diuretic
effect of the drug occurs in
approximately 2.6 hours and continues for up to 72 hours. The mean
half-life following a 50 to 200 mg
dose is 40 hours. In the first order of absorption, the elimination
half-life is 53 hours following a 50
mg dose, and 60 hours following a 100 mg dose. Approximately 75
percent of the drug is bound to
plasma proteins, 58 percent of the drug being bound to albumin. This
is caused by an increased affinity
of the drug to erythrocyte carbonic anhydrase. Nonrenal routes of
elimination have yet to be clarified.
Data are not available regarding percentage of dose as unchanged drug
and metabolites, concentration
of the drug in body fluids, degree of uptake by a particular organ or
in the fetus, or passage across the
blood-brain barrier.
The drug produces copious diuresis with greatly increased excretion of
sodium and chloride. At
maximal therapeutic dosage, chlorthalidone is approximately equal in
its diuretic effect to comparable
maximal therapeuti