Chlorothiazide

Chlorothiazide Sodium


Fresenius Kabi Usa, Llc
Human Prescription Drug
NDC 63323-658
Chlorothiazide also known as Chlorothiazide Sodium is a human prescription drug labeled by 'Fresenius Kabi Usa, Llc'. National Drug Code (NDC) number for Chlorothiazide is 63323-658. This drug is available in dosage form of Injection, Powder, Lyophilized, For Solution. The names of the active, medicinal ingredients in Chlorothiazide drug includes Chlorothiazide Sodium - 500 mg/18mL . The currest status of Chlorothiazide drug is Active.

Drug Information:

Drug NDC: 63323-658
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Chlorothiazide
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Chlorothiazide Sodium
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Fresenius Kabi Usa, Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Injection, Powder, Lyophilized, For Solution
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:CHLOROTHIAZIDE SODIUM - 500 mg/18mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:INTRAVENOUS
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: ANDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 21 Oct, 2009
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 17 Jan, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: ANDA090896
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.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Fresenius Kabi USA, LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:484152
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UNII:SN86FG7N2K
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Increased Diuresis [PE]
Thiazide Diuretic [EPC]
Thiazides [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63323-658-271 VIAL in 1 BOX (63323-658-27) / 18 mL in 1 VIAL21 Oct, 2009N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Chlorothiazide chlorothiazide sodium chlorothiazide sodium chlorothiazide mannitol sodium hydroxide

Indications and Usage:

Indications and usage: chlorothiazide sodium for injection is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. chlorothiazide sodium for injection has also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. 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.

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 a
ssociated 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.

Warnings:

Warnings: intravenous use in infants and children has been limited and is not generally recommended. 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 ) .

Dosage and Administration:

Dosage and administration: chlorothiazide sodium for injection should be reserved for patients unable to take oral medication or for emergency situations. therapy should be individualized according to patient response. use the smallest dosage necessary to achieve the required response. intravenous use in infants and children has been limited and is not generally recommended. when medication can be taken orally, therapy with chlorothiazide tablets or oral suspension may be substituted for intravenous therapy, using the same dosage schedule as for the parenteral route. chlorothiazide sodium for injection may be given slowly by direct intravenous injection or by intravenous infusion. extravasation must be rigidly avoided. do not give subcutaneously or intramuscularly. the usual adult dosage is 500 mg to 1 g once or twice a day. many patients with edema respond to intermittent therapy, i.e., administration on alternate days or on three to five days each week. with an intermittent schedule,
excessive response and the resulting undesirable electrolyte imbalance are less likely to occur. directions for reconstitution use aseptic technique. because chlorothiazide sodium for injection contains no preservative, a fresh solution should be prepared immediately prior to each administration, and the unused portion should be discarded. add 18 ml of sterile water for injection to the vial to form an isotonic solution for intravenous injection. never add less than 18 ml. when reconstituted with 18 ml of sterile water, the final concentration of intravenous chlorothiazide sodium is 28 mg/ml. the reconstituted solution is clear and essentially free from visible particles. parenteral drug products should be inspected visually for particulate matter and discoloration prior to use whenever solution and container permit. the solution is compatible with dextrose or sodium chloride solutions for intravenous infusion. avoid simultaneous administration of solutions of chlorothiazide with whole blood or its derivatives.

Directions for reconstitution use aseptic technique. because chlorothiazide sodium for injection contains no preservative, a fresh solution should be prepared immediately prior to each administration, and the unused portion should be discarded. add 18 ml of sterile water for injection to the vial to form an isotonic solution for intravenous injection. never add less than 18 ml. when reconstituted with 18 ml of sterile water, the final concentration of intravenous chlorothiazide sodium is 28 mg/ml. the reconstituted solution is clear and essentially free from visible particles. parenteral drug products should be inspected visually for particulate matter and discoloration prior to use whenever solution and container permit. the solution is compatible with dextrose or sodium chloride solutions for intravenous infusion. avoid simultaneous administration of solutions of chlorothiazide with whole blood or its derivatives.

Contraindications:

Contraindications: anuria. hypersensitivity to any component of this product or to other sulfonamide-derived drugs.

Adverse Reactions:

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, re
stlessness. skin - erythema multiforme including stevens-johnson syndrome, exfoliative dermatitis including toxic epidermal necrolysis, alopecia. special senses - transient blurred vision, xanthopsia. renal - renal failure, renal dysfunction, interstitial nephritis, (see warnings ); hematuria (following intravenous use). urogenital - impotence. whenever adverse reactions are moderate or severe, thiazide dosage should be reduced or therapy withdrawn.

Overdosage:

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. 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 chlorothiazide sodium is removed by hemodialysis has not been established. the intravenous ld 50 of chlorothiazide in the mouse is 1.1 g/kg.

Description:

Description: chlorothiazide sodium for injection, usp is a diuretic and antihypertensive. it is 6-chloro-2 h -1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide monosodium salt, and its structural formula is: c 7 h 5 cln 3 nao 4 s 2 m.w. 317.71 chlorothiazide sodium for injection, usp is a sterile lyophilized white powder and is supplied in a vial containing: chlorothiazide sodium equivalent to chlorothiazide 500 mg, and the inactive ingredient mannitol 250 mg with sodium hydroxide to adjust ph. chlorothiazide is a diuretic and antihypertensive. it is 6-chloro-2 h -1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide, and its structural formula is: c 7 h 6 cln 3 o 4 s 2 m.w. 295.72 it is a white, or practically white, crystalline powder, which is very slightly soluble in water, but readily soluble in dilute aqueous sodium hydroxide. it is soluble in urine to the extent of about 150 mg per 100 ml at ph 7. structure 1 structure 2

Clinical Pharmacology:

Clinical pharmacology: the mechanism of the antihypertensive effect of thiazides is unknown. chlorothiazide does not usually affect normal blood pressure. chlorothiazide affects the distal renal tubular mechanism of electrolyte reabsorption. at maximal therapeutic dosage all thiazides are approximately equal in their diuretic efficacy. chlorothiazide 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. following intravenous use of chlorothiazide sodium, onset of the diuretic action occurs in 15 minutes and the maximal action in 30 minutes. pharmacokinetics and metabolism chlorothiazide is not metabolized but is eliminated rapidly by the kidney; 96 percent of an intravenous dose is excreted unchanged in the urine within 23 hours. the plasma half-life of chlorothiazide is 45 to 120 minutes
. chlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.

Pharmacokinetics:

Pharmacokinetics and metabolism chlorothiazide is not metabolized but is eliminated rapidly by the kidney; 96 percent of an intravenous dose is excreted unchanged in the urine within 23 hours. the plasma half-life of chlorothiazide is 45 to 120 minutes. chlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.

How Supplied:

How supplied: chlorothiazide sodium for injection, usp is a dry, sterile lyophilized powder, supplied as follows: product no. ndc no. strength np605820 63323-658-27 500 mg per vial packaged individually. the container closure is not made with natural rubber latex. storage store lyophilized powder between: 2 ° and 25 °c ( 36 ° and 77 °f). for single dose only. use solution immediately after reconstitution. (see dosage and administration , directions for reconstitution .) discard unused portion of the reconstituted solution. novaplus is a registered trademark of vizient, inc.

Storage store lyophilized powder between: 2 ° and 25 °c ( 36 ° and 77 °f). for single dose only. use solution immediately after reconstitution. (see dosage and administration , directions for reconstitution .) discard unused portion of the reconstituted solution. novaplus is a registered trademark of vizient, inc.

Package Label Principal Display Panel:

Package label - prinicipal display - chlorothiazide 500 mg* per vial label chlorothiazide sodium for injection, usp 500 mg* per vial for the preparation of intravenous solutions. single dose vial rx only package label - prinicipal display - chlorothiazide 500 mg* per vial carton panel chlorothiazide sodium for injection, usp 500 mg* per vial for the preparation of intravenous solutions. rx only single dose vial vial pbox


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