Lidocaine Hydrochloride


Morton Grove Pharmaceuticals, Inc.
Human Prescription Drug
NDC 60432-465
Lidocaine Hydrochloride is a human prescription drug labeled by 'Morton Grove Pharmaceuticals, Inc.'. National Drug Code (NDC) number for Lidocaine Hydrochloride is 60432-465. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Lidocaine Hydrochloride drug includes Lidocaine Hydrochloride - 40 mg/mL . The currest status of Lidocaine Hydrochloride drug is Active.

Drug Information:

Drug NDC: 60432-465
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: Lidocaine 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: Lidocaine Hydrochloride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Morton Grove Pharmaceuticals, Inc.
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:LIDOCAINE HYDROCHLORIDE - 40 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
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: 18 Nov, 1982
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 20 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: ANDA087881
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:Morton Grove Pharmaceuticals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:1010878
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:V13007Z41A
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:Amide Local Anesthetic [EPC]
Amides [CS]
Antiarrhythmic [EPC]
Local Anesthesia [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
60432-465-511 BOTTLE, GLASS in 1 CARTON (60432-465-51) / 50 mL in 1 BOTTLE, GLASS (60432-465-50)18 Nov, 1982N/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:

Lidocaine hydrochloride lidocaine hydrochloride lidocaine hydrochloride lidocaine lidocaine hydrochloride anhydrous propylene glycol methylparaben water sodium hydroxide

Indications and Usage:

Indications and usage lidocaine hydrochloride topical solution is indicated for the production of topical anesthesia of accessible mucous membranes of the oral and nasal cavities and proximal portions of the digestive tract.

Warnings:

Warnings in order to manage possible adverse reactions, resuscitative equipment, oxygen and other resuscitative drugs must be immediately available when local anesthetic agents, such as lidocaine, are administered to mucous membranes. lidocaine hydrochloride topical solution usp 4% should be used with extreme caution if there is sepsis or severely traumatized mucosa in the area of application, since under such conditions there is the potential for rapid systemic absorption. methemoglobinemia cases of methemoglobinemia have been reported in association with local anesthetic use. although all patients are at risk for methemoglobinemia, patients with glucose-6-phosphate dehydrogenase deficiency, congenital or idiopathic methemoglobinemia, cardiac or pulmonary compromise, infants under 6 months of age, and concurrent exposure to oxidizing agents or their metabolites are more susceptible to developing clinical manifestations of the condition. if local anesthetics must be used in these patie
nts, close monitoring for symptoms and signs of methemoglobinemia is recommended. signs and symptoms of methemoglobinemia may occur immediately or may be delayed some hours after exposure, and are characterized by a cyanotic skin discoloration and abnormal coloration of the blood. methemoglobin levels may continue to rise; therefore, immediate treatment is required to avert more serious central nervous system and cardiovascular adverse effects, including seizures, coma, arrhythmias, and death. discontinue lidocaine and any other oxidizing agents. depending on the severity of the symptoms, patients may respond to supportive care, i.e., oxygen therapy, hydration. more severe symptoms may require treatment with methylene blue, exchange transfusion, or hyperbaric oxygen.

Dosage and Administration:

Dosage and administration when lidocaine hydrochloride topical solution, usp 4% is used concomitantly with other products containing lidocaine, the total dose contributed by all formulations must be kept in mind. the dosage varies and depends upon the area to be anesthetized, vascularity of the tissues, individual tolerance, and the technique of anesthesia. the lowest dosage needed to provide effective anesthesia should be administered. dosages should be reduced for children and for elderly and debilitated patients. although the incidence of adverse effects with lidocaine hydrochloride is quite low, caution should be exercised, particularly when employing large volumes, since the incidence of adverse effects is directly proportional to the total dose of local anesthetic agent administered. the dosages recommended below are for normal, healthy adults: when used as a spray, or when applied by means of cotton applicators or packs, as when instilled into a cavity, the suggested dosage of l
idocaine hydrochloride topical solution is 1 to 5 ml (40 to 200 mg lidocaine hydrochloride), i.e., 0.6 to 3.0 mg/kg or 0.3 to 1.5 mg/lb body weight. note: the solution may be applied with a sterile swab which is discarded after a single use and never reused under any circumstances. when spraying, transfer the solution from the original container to an atomizer.

Contraindications:

Contraindications lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type, or to other components of lidocaine hydrochloride topical solution.

Adverse Reactions:

Adverse reactions adverse experiences following the administration of lidocaine are similar in nature to those observed with other amide local anesthetic agents. these adverse experiences are, in general, dose-related and may result from high plasma levels caused by excessive dosage or rapid absorption, or may result from a hypersensitivity, idiosyncrasy or diminished tolerance on the part of the patient. serious adverse experiences are generally systemic in nature. the following types are those most commonly reported: central nervous system cns manifestations are excitatory and/or depressant and may be characterized by lightheadedness, nervousness, apprehension, euphoria, confusion, dizziness, drowsiness, tinnitus, blurred or double vision, vomiting, sensations of heat, cold or numbness, twitching, tremors, convulsions, unconsciousness, respiratory depression and arrest. the excitatory manifestations may be very brief or may not occur at all, in which case the first manifestation of t
oxicity may be drowsiness merging into unconsciousness and respiratory arrest. drowsiness following the administration of lidocaine is usually an early sign of a high blood level of the drug and may occur as a consequence of rapid absorption. cardiovascular system cardiovascular manifestations are usually depressant and are characterized by bradycardia, hypotension, and cardiovascular collapse, which may lead to cardiac arrest. allergic allergic reactions are characterized by cutaneous lesions, urticaria, edema or anaphylactoid reactions. allergic reactions as a result of sensitivity to lidocaine are extremely rare and, if they occur, should be managed by conventional means. the detection of sensitivity by skin testing is of doubtful value.

Pediatric Use:

Pediatric use dosages in pediatric patients should be reduced, commensurate with age, body weight and physical condition. see dosage and administration .

Overdosage:

Overdosage acute emergencies from local anesthetics are generally related to high plasma levels encountered during therapeutic use of local anesthetics. (see adverse reactions , warnings , and precautions ). management of local anesthetic emergencies the first consideration is prevention, best accomplished by careful and constant monitoring of cardiovascular and respiratory vital signs and the patient's state of consciousness after each local anesthetic administration. at the first sign of change, oxygen should be administered. the first step in the management of convulsions consists of immediate attention to the maintenance of a patent airway and assisted or controlled ventilation with oxygen and a delivery system capable of permitting immediate positive airway pressure by mask. immediately after the institution of these ventilatory measures, the adequacy of the circulation should be evaluated, keeping in mind that drugs used to treat convulsions sometimes depress the circulation when administered intravenously. should convulsions persist despite adequate respiratory support, and if the status of the circulation permits, small increments of an ultra-short acting barbiturate (such as thiopental or thiamylal) or a benzodiazepine (such as diazepam) may be administered intravenously. the clinician should be familiar, prior to use of local anesthetics, with these anticonvulsant drugs. supportive treatment of circulatory depression may require administration of intravenous fluids and, when appropriate, a vasopressor as directed by the clinical situation (e.g., ephedrine). if not treated immediately, both convulsions and cardiovascular depression can result in hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest. if cardiac arrest should occur, standard cardiopulmonary resuscitative measures should be instituted. dialysis is of negligible value in the treatment of acute overdosage with lidocaine. the intravenous ld 50 of lidocaine hydrochloride in female mice is 26 (21 to 31) mg/kg and the subcutaneous ld 50 is 264 (203 to 304) mg/kg.

Description:

Description lidocaine hydrochloride topical solution, usp 4% contains a local anesthetic agent and is administered topically. see indications for specific uses. lidocaine hydrochloride topical solution usp 4% contains lidocaine hydrochloride monohydrate, which is chemically designated as 2-(diethylamino)-2',6'-acetoxylidide monohydrochloride monohydrate and has the following structural formula: c 14 h 22 n 2 o ∙ hcl ∙ h 2 0 m.w. 288.81 each ml contains: lidocaine hydrochloride monohydrate, 40 usp mg inactive ingredients: methylparaben, propylene glycol and purified water. it may also contain sodium hydroxide for ph adjustment. the ph range is between 5.0 and 7.0. an aqueous solution for topical use only. not for injection. lidocaine-01

Clinical Pharmacology:

Clinical pharmacology mechanism of action lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses, thereby effecting local anesthetic action. hemodynamics excessive blood levels may cause changes in cardiac output, total peripheral resistance, and mean arterial pressure. these changes may be attributable to a direct depressant effect of the local anesthetic agent on various components of the cardiovascular system. the net effect is normally a modest hypotension when the recommended dosages are not exceeded. pharmacokinetics and metabolism information derived from other formulations, concentrations and usages reveals that lidocaine is completely absorbed following parenteral administration, its rate of absorption depending, for example, upon such factors such as the site of administration and the presence or absence of a vasoconstrictor agent. lidocaine may be absorbed following topical administration to mucous mem
branes, its rate of absorption and percent of dose absorbed depending upon concentration and total dose administered, the specific site of application and duration of exposure. in general, the rate of absorption of local anesthetic agents following topical application occurs most rapidly after intratracheal administration. lidocaine is also well-absorbed from the gastrointestinal tract, but little intact drug appears in the circulation because of biotransformation by the liver. lidocaine is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the kidneys. biotransformation includes oxidative n-dealkylation, ring hydroxylation, cleavage of the amide linkage, and conjugation. n-dealkylation, a major pathway of biotransformation, yields the metabolites monoethylglycinexylidide and glycinexylidide. the pharmacological/toxicological actions of these metabolites are similar to, but less potent than, those of lidocaine. approximately 90% of lidocaine administered is excreted in the form of various metabolites, and less than 10% is excreted unchanged. the primary metabolite in urine is a conjugate of 4-hydroxy-2, 6-dimethylaniline. studies have shown that peak blood levels of lidocaine may occur as early as 5 and as late as 30 minutes after endotracheal administration of a 4% lidocaine hcl solution. the plasma binding of lidocaine is dependent on drug concentration, and the fraction bound decreases with increasing concentration. at concentrations of 1 to 4 mcg of free base per ml, 60 to 80 percent of lidocaine is protein bound. binding is also dependent on the plasma concentration of the alpha-1-acid glycoprotein. lidocaine crosses the blood-brain and placental barriers, presumably by passive diffusion. studies of lidocaine metabolism following intravenous bolus injections have shown that the elimination half-life of this agent is typically 1.5 to 2.0 hours. because of the rapid rate at which lidocaine is metabolized, any condition that affects liver function may alter lidocaine kinetics. the half-life may be prolonged two-fold or more in patients with liver dysfunction. renal dysfunction does not affect lidocaine kinetics but may increase the accumulation of metabolites. factors such as acidosis and the use of cns stimulants and depressants affect the cns levels of lidocaine required to produce overt systemic effects. objective adverse manifestations become increasingly apparent with increasing venous plasma levels above 6.0 mcg free base per ml. in the rhesus monkey arterial blood levels of 18 to 21 mcg/ml have been shown to be threshold for convulsive activity.

Mechanism of Action:

Mechanism of action lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses, thereby effecting local anesthetic action.

How Supplied:

How supplied lidocaine hydrochloride topical solution, usp 4% is supplied in 50 ml bottle (ndc 60432-465-50) and packaged in a carton (ndc 60432-465-51). an aqueous solution for topical application. not for injection. recommended storage store at 20 ° to 25 °c (68 ° to 77 °f) [see usp controlled room temperature]. avoid freezing rx only product no.: 8465 manufactured by: morton grove pharmaceuticals, inc. morton grove, il 60053 manufactured for: wockhardt usa, llc parsippany, nj 07054 28465 rev. 06-20

Information for Patients:

Information for patients when topical anesthetics are used in the mouth, the patient should be aware that the production of topical anesthesia may impair swallowing and thus enhance the danger of aspiration. for this reason, food should not be ingested for 60 minutes following use of local anesthetic preparations in the mouth or throat area. this is particularly important in children because of their frequency of eating. numbness of the tongue or buccal mucosa may enhance the danger of unintentional biting trauma. food and chewing gum should not be taken while the mouth or throat area is anesthetized. inform patients that use of local anesthetics may cause methemoglobinemia, a serious condition that must be treated promptly. advise patients or caregivers to stop use and seek immediate medical attention if they or someone in their care experience the following signs or symptoms: pale, gray, or blue colored skin (cyanosis); headache; rapid heart rate; shortness of breath; lightheadedness
; or fatigue.

Package Label Principal Display Panel:

Principal display panel mgp ndc 60432-465-51 lidocaine hydrochloride topical solution, usp 4% not for injection topical use only rx only net: 1 ⅔ fl oz (50 ml) carton-r1222 carton label


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