Promethazine Hydrochloride

Promethazine


Amneal Pharmaceuticals Llc
Human Prescription Drug
NDC 65162-678
Promethazine Hydrochloride also known as Promethazine is a human prescription drug labeled by 'Amneal Pharmaceuticals Llc'. National Drug Code (NDC) number for Promethazine Hydrochloride is 65162-678. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Promethazine Hydrochloride drug includes Promethazine Hydrochloride - 6.25 mg/5mL . The currest status of Promethazine Hydrochloride drug is Active.

Drug Information:

Drug NDC: 65162-678
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: Promethazine Hydrochloride
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: Promethazine
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Amneal Pharmaceuticals Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: 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:PROMETHAZINE HYDROCHLORIDE - 6.25 mg/5mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
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: 30 Dec, 2009
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 02 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: ANDA040882
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:Amneal Pharmaceuticals LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:992432
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:R61ZEH7I1I
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:Phenothiazine [EPC]
Phenothiazines [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
65162-678-86118 mL in 1 BOTTLE (65162-678-86)30 Dec, 2009N/ANo
65162-678-90473 mL in 1 BOTTLE (65162-678-90)30 Dec, 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:

Promethazine hydrochloride promethazine promethazine hydrochloride promethazine alcohol ascorbic acid citric acid monohydrate d&c yellow no. 10 edetate disodium fd&c blue no. 1 glycerin methylparaben saccharin sodium sodium benzoate sodium citrate sucrose clear

Indications and Usage:

Indications and usage promethazine hcl oral solution is useful for: perennial and seasonal allergic rhinitis. vasomotor rhinitis. allergic conjunctivitis due to inhalant allergens and foods. mild, uncomplicated allergic skin manifestations of urticaria and angioedema. amelioration of allergic reactions to blood or plasma. dermographism. anaphylactic reactions, as adjunctive therapy to epinephrine and other standard measures, after the acute manifestations have been controlled. preoperative, postoperative, or obstetric sedation. prevention and control of nausea and vomiting associated with certain types of anesthesia and surgery. therapy adjunctive to meperidine or other analgesics for control of post-operative pain. sedation in both children and adults, as well as relief of apprehension and production of light sleep from which the patient can be easily aroused. active and prophylactic treatment of motion sickness. antiemetic therapy in postoperative patients.

Warnings:

Warnings promethazine hcl oral solution should not be used in pediatric patients less than 2 years of age because of the potential for fatal respiratory depression. postmarketing cases of respiratory depression, including fatalities, have been reported with use of promethazine in pediatric patients less than 2 years of age. a wide range of weight-based doses of promethazine have resulted in respiratory depression in these patients. caution should be exercised when administering promethazine to pediatric patients 2 years of age and older. it is recommended that the lowest effective dose of promethazine be used in pediatric patients 2 years of age and older and concomitant administration of other drugs with respiratory depressant effects be avoided. cns depression promethazine hcl oral solution may impair the mental and/or physical abilities required for the performance of potentially hazardous tasks, such as driving a vehicle or operating machinery. the impairment may be amplified by co
ncomitant use of other central-nervous-system depressants such as alcohol, sedatives/hypnotics (including barbiturates), narcotics, narcotic analgesics, general anesthetics, tricyclic antidepressants, and tranquilizers; therefore such agents should either be eliminated or given in reduced dosage in the presence of promethazine hcl (see precautions - information for patients and drug interactions ). respiratory depression promethazine hcl oral solution may lead to potentially fatal respiratory depression. use of promethazine hcl oral solution in patients with compromised respiratory function (e.g., copd, sleep apnea) should be avoided. lower seizure threshold promethazine hcl oral solution may lower seizure threshold. it should be used with caution in persons with seizure disorders or in persons who are using concomitant medications, such as narcotics or local anesthetics, which may also affect seizure threshold. bone-marrow depression promethazine hcl oral solution should be used with caution in patients with bone-marrow depression. leukopenia and agranulocytosis have been reported, usually when promethazine hcl oral solution has been used in association with other known marrow-toxic agents. neuroleptic malignant syndrome a potentially fatal symptom complex sometimes referred to as neuroleptic malignant syndrome (nms) has been reported in association with promethazine hcl alone or in combination with antipsychotic drugs. clinical manifestations of nms are hyperpyrexia, muscle rigidity, altered mental status and evidence of autonomic instability (irregular pulse or blood pressure, tachycardia, diaphoresis and cardiac dysrhythmias). the diagnostic evaluation of patients with this syndrome is complicated. in arriving at a diagnosis, it is important to identify cases where the clinical presentation includes both serious medical illness (e.g., pneumonia, systemic infection, etc.) and untreated or inadequately treated extrapyramidal signs and symptoms (eps). other important considerations in the differential diagnosis include central anticholinergic toxicity, heat stroke, drug fever and primary central nervous system (cns) pathology. the management of nms should include 1) immediate discontinuation of promethazine hcl, antipsychotic drugs, if any, and other drugs not essential to concurrent therapy, 2) intensive symptomatic treatment and medical monitoring, and 3) treatment of any concomitant serious medical problems for which specific treatments are available. there is no general agreement about specific pharmacological treatment regimens for uncomplicated nms. since recurrences of nms have been reported with phenothiazines, the reintroduction of promethazine hcl should be carefully considered. use in pediatric patients promethazine hcl oral solution is contraindicated for use in pediatric patients less than two years of age. caution should be exercised when administering promethazine hcl oral solution to pediatric patients 2 years of age and older because of the potential for fatal respiratory depression. respiratory depression and apnea, sometimes associated with death, are strongly associated with promethazine products and are not directly related to individualized weight-based dosing, which might otherwise permit safe administration. concomitant administration of promethazine products with other respiratory depressants has an association with respiratory depression, and sometimes death, in pediatric patients. antiemetics are not recommended for treatment of uncomplicated vomiting in pediatric patients, and their use should be limited to prolonged vomiting of known etiology. the extrapyramidal symptoms which can occur secondary to promethazine hcl oral solution administration may be confused with the cns signs of undiagnosed primary disease, e.g., encephalopathy or reye’s syndrome. the use of promethazine hcl oral solution should be avoided in pediatric patients whose signs and symptoms may suggest reye’s syndrome or other hepatic diseases. excessively large dosages of antihistamines, including promethazine hcl oral solution, in pediatric patients may cause sudden death (see overdosage ). hallucinations and convulsions have occurred with therapeutic doses and overdoses of promethazine hcl oral solution in pediatric patients. in pediatric patients who are acutely ill associated with dehydration, there is an increased susceptibility to dystonias with the use of promethazine hcl. other considerations administration of promethazine hci has been associated with reported cholestatic jaundice.

Dosage and Administration:

Dosage and administration it is important that promethazine hcl oral solution is measured with an accurate measuring device (see precautions – information for patients). a household teaspoon is not an accurate measuring device and could lead to overdosage, especially when half a teaspoon is to be measured. it is strongly recommended that an accurate measuring device be used. a pharmacist can provide an appropriate device and can provide instructions for measuring the correct dose. promethazine hcl oral solution is contraindicated for children under 2 years of age (see warnings – boxed warning and use in pediatric patients). allergy the average oral dose is 25 mg taken before retiring; however, 12.5 mg may be taken before meals and on retiring, if necessary. single 25 mg doses at bedtime or 6.25 to 12.5 mg taken three times daily will usually suffice. after initiation of treatment in children or adults, dosage should be adjusted to the smallest amount adequate to relieve sympt
oms. the administration of promethazine hci in 25 mg doses will control minor transfusion reactions of an allergic nature. motion sickness the average adult dose is 25 mg taken twice daily. the initial dose should be taken one-half to one hour before anticipated travel and be repeated 8 to 12 hours later, if necessary. on succeeding days of travel, it is recommended that 25 mg be taken on arising and again before the evening meal. for children, 12.5 to 25 mg, twice daily, may be administered. nausea and vomiting antiemetics should not be used in vomiting of unknown etiology in children and adolescents (see warnings-use in pediatric patients). the average effective dose of promethazine hcl oral solution for the active therapy of nausea and vomiting in children or adults is 25 mg. when oral medication cannot be tolerated, the dose should be given parenterally (cf. promethazine hydrochloride injection) or by rectal suppository. 12.5 to 25 mg doses may be repeated, as necessary, at 4 to 6 hour intervals. for nausea and vomiting in children, the usual dose is 0.5 mg per pound of body weight, and the dose should be adjusted to the age and weight of the patient and the severity of the condition being treated. for prophylaxis of nausea and vomiting, as during surgery and the postoperative period, the average dose is 25 mg repeated at 4 to 6 hour intervals, as necessary. sedation this product relieves apprehension and induces a quiet sleep from which the patient can be easily aroused. administration of 12.5 to 25 mg promethazine hcl oral solution by the oral route will provide sedation in children. adults usually require 25 to 50 mg for nighttime, presurgical, or obstetrical sedation. pre- and postoperative use promethazine hcl oral solution in 12.5 to 25 mg doses for children and 50 mg doses for adults the night before surgery relieves apprehension and produces a quiet sleep. for preoperative medication, children require doses of 0.5 mg per pound of body weight in combination with an appropriately reduced dose of narcotic or barbiturate and the appropriate dose of an atropine-like drug. usual adult dosage is 50 mg promethazine hcl oral solution with an appropriately reduced dose of narcotic or barbiturate and the required amount of a belladonna alkaloid. postoperative sedation and adjunctive use with analgesics may be obtained by the administration of 12.5 to 25 mg in children and 25 to 50 mg doses in adults. promethazine hcl oral solution is contraindicated for children under 2 years of age.

Contraindications:

Contraindications promethazine hcl oral solution is contraindicated for use in pediatric patients less than two years of age. promethazine hcl oral solution is contraindicated in comatose states, and in individuals known to be hypersensitive or to have had an idiosyncratic reaction to promethazine or to other phenothiazines. antihistamines are contraindicated for use in the treatment of lower respiratory tract symptoms including asthma.

Adverse Reactions:

Adverse reactions central nervous system - drowsiness is the most prominent cns effect of this drug. sedation, somnolence, blurred vision, dizziness, confusion, disorientation, and extrapyramidal symptoms such as oculogyric crisis, torticollis, and tongue protrusion; lassitude, tinnitus, incoordination, fatigue, euphoria, nervousness, diplopia, insomnia, tremors, convulsive seizures, excitation, catatonic-like states, hysteria. hallucinations have also been reported. cardiovascular-increased or decreased blood pressure, tachycardia, bradycardia, faintness. dermatologic-dermatitis, photosensitivity, urticaria. hematologic-leukopenia, thrombocytopenia, thrombocytopenic purpura, agranulocytosis. gastrointestinal-dry mouth, nausea, vomiting, jaundice. respiratory-asthma, nasal stuffiness, respiratory depression (potentially fatal) and apnea (potentially fatal) (see warnings-respiratory depression ). other-angioneurotic edema. neuroleptic malignant syndrome (potentially fatal) has also been
reported (see warnings-neuroleptic malignant syndrome ). to report suspected adverse reactions, contact amneal pharmaceuticals at 1-877-835-5472 or fda at 1-800-fda-1088 or www.fda.gov/medwatch. paradoxical reactions hyperexcitability and abnormal movements have been reported in patients following a single administration of promethazine hci. consideration should be given to the discontinuation of promethazine hci and to the use of other drugs if these reactions occur. respiratory depression, nightmares, delirium, and agitated behavior have also been reported in some of these patients.

Overdosage:

Overdosage signs and symptoms of overdosage with promethazine hci range from mild depression of the central nervous system and cardiovascular system to profound hypotension, respiratory depression, unconsciousness, and sudden death. other reported reactions include hyperreflexia, hypertonia, ataxia, athetosis, and extensor-plantar reflexes (babinski reflex). stimulation may be evident, especially in children and geriatric patients. convulsions may rarely occur. a paradoxical-type reaction has been reported in children receiving single doses of 75 mg to 125 mg orally, characterized by hyperexcitability and nightmares. atropine-like signs and symptoms-dry mouth, fixed, dilated pupils, flushing, as well as gastrointestinal symptoms-may occur. treatment treatment of overdosage is essentially symptomatic and supportive. only in cases of extreme overdosage or individual sensitivity do vital signs, including respiration, pulse, blood pressure, temperature, and ekg, need to be monitored. activated charcoal orally or by lavage may be given, or sodium or magnesium sulfate orally as a cathartic. attention should be given to the reestablishment of adequate respiratory exchange through provision of a patent airway and institution of assisted or controlled ventilation. diazepam may be used to control convulsions. acidosis and electrolyte losses should be corrected. note that any depressant effects of promethazine hci are not reversed by naloxone. avoid analeptics which may cause convulsions. the treatment of choice for resulting hypotension is administration of intravenous fluids, accompanied by repositioning if indicated. in the event that vasopressors are considered for the management of severe hypotension which does not respond to intravenous fluids and repositioning, the administration of norepinephrine or phenylephrine should be considered. epinephrine should not be used, since its use in patients with partial adrenergic blockade may further lower the blood pressure. extrapyramidal reactions may be treated with anticholinergic antiparkinsonian agents, diphenhydramine, or barbiturates.oxygen may also be administered. limited experience with dialysis indicates that it is not helpful.

Description:

Description each teaspoonful (5 ml) of promethazine hcl oral solution, usp contains 6.25 mg of promethazine hcl, usp in a flavored syrup base with a ph between 4.7 and 5.2. alcohol 7%. the inactive ingredients present are alcohol, ascorbic acid, citric acid, d&c yellow # 10, edetate disodium, fd&c blue # 1, glycerin, methylparaben, natural and artificial banana flavor, natural and artificial fruit flavor, saccharin sodium, sodium benzoate, sodium citrate, and sucrose. promethazine hcl, usp is a racemic compound; the molecular formula is c 17 h 20 n 2 s•hcl and its molecular weight is 320.88. promethazine hcl usp, a phenothiazine derivative, is designated chemically as 10 h -phenothiazine-10-ethanamine, n,n , α-trimethyl-, monohydrochloride, (±)- with the following structural formula: promethazine hcl, usp occurs as a white to faint yellow, practically odorless, crystalline powder which slowly oxidizes and turns blue on prolonged exposure to air. it is freely soluble in water and soluble in alcohol. d81951c9-figure-01

Clinical Pharmacology:

Clinical pharmacology promethazine is a phenothiazine derivative which differs structurally from the antipsychotic phenothiazines by the presence of a branched side chain and no ring substitution. it is thought that this configuration is responsible for its relative lack (1/10 that of chlorpromazine) of dopamine antagonist properties. promethazine is an h 1 receptor blocking agent. in addition to its antihistaminic action, it provides clinically useful sedative and antiemetic effects. promethazine is well absorbed from the gastrointestinal tract. clinical effects are apparent within 20 minutes after oral administration and generally last four to six hours, although they may persist as long as 12 hours. promethazine is metabolized by the liver to a variety of compounds; the sulfoxides of promethazine and n-demethylpromethazine are the predominant metabolites appearing in the urine.

How Supplied:

How supplied promethazine hcl oral solution usp, 6.25 mg/5 ml , is a clear, green colored solution. it is available as follows: 4 fl oz (118 ml) ndc 65162-678-86 16 fl oz (473 ml) ndc 65162-678-90 keep tightly closed. store at 20° to 25°c (68° to 77°f) [see usp controlled room temperature]. protect from light. dispense in tight, light-resistant container as defined in the usp, with a child-resistant closure. distributed by: amneal pharmaceuticals llc bridgewater, nj 08807 rev. 12-2019-00

Package Label Principal Display Panel:

Package label.principal display panel 4 oz label 16 oz label


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.