Nafcillin

Nafcillin Sodium


Athenex Pharmaceutical Division, Llc.
Human Prescription Drug
NDC 70860-117
Nafcillin also known as Nafcillin Sodium is a human prescription drug labeled by 'Athenex Pharmaceutical Division, Llc.'. National Drug Code (NDC) number for Nafcillin is 70860-117. This drug is available in dosage form of Powder, For Solution. The names of the active, medicinal ingredients in Nafcillin drug includes Nafcillin Sodium - 2 g/1 . The currest status of Nafcillin drug is Active.

Drug Information:

Drug NDC: 70860-117
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: Nafcillin
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: Nafcillin Sodium
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Athenex Pharmaceutical Division, Llc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Powder, 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:NAFCILLIN SODIUM - 2 g/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:INTRAMUSCULAR
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: 01 Aug, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 21 Dec, 2025
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: ANDA090560
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:Athenex Pharmaceutical Division, LLC.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:1721458
1721460
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:49G3001BCK
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:Penicillin-class Antibacterial [EPC]
Penicillins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
70860-117-2610 VIAL in 1 CARTON (70860-117-26) / 1 POWDER, FOR SOLUTION in 1 VIAL (70860-117-41)01 Aug, 2018N/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:

Nafcillin nafcillin sodium nafcillin sodium nafcillin nafcillin nafcillin sodium nafcillin sodium nafcillin

Drug Interactions:

Drug interactions tetracycline, a bacteriostatic antibiotic, may antagonize the bactericidal effect of penicillin, and concurrent use of these drugs should be avoided. nafcillin in high dosage regimens, i.e., 2 grams every 4 hours, has been reported to decrease the effects of warfarin. when nafcillin and warfarin are used concomitantly, the prothrombin time should be closely monitored and the dose of warfarin adjusted as necessary. this effect may persist for up to 30 days after nafcillin has been discontinued. nafcillin when administered concomitantly with cyclosporine has been reported to result in subtherapeutic cyclosporine levels. the nafcillin-cyclosporine interaction was documented in a patient during two separate courses of therapy. when cyclosporine and nafcillin are used concomitantly in organ transplant patients, the cyclosporine levels should be monitored.

Indications and Usage:

Indications and usage nafcillin is indicated in the treatment of infections caused by penicillinase-producing staphylococci which have demonstrated susceptibility to the drug. culture and susceptibility tests should be performed initially to determine the causative organism and its susceptibility to the drug (see clinical pharmacology - susceptibility test methods ). nafcillin should not be used in infections caused by organisms susceptible to penicillin g. if the susceptibility tests indicate that the infection is due to methicillin-resistant staphylococcus sp., therapy with nafcillin for injection should be discontinued and alternative therapy provided. to reduce the development of drug-resistant bacteria and maintain the effectiveness of nafcillin for injection and other antibacterial drugs, nafcillin for injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. when culture and susceptibility information
are available, they should be considered in selecting or modifying antibacterial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Warnings:

Warnings serious and occasionally fatal hypersensitivity (anaphylactic) reactions have been reported in patients on penicillin therapy. these reactions are more likely to occur in individuals with a history of penicillin hypersensitivity and/or a history of sensitivity to multiple allergens. before initiating therapy with nafcillin, careful inquiry should be made concerning previous hypersensitivity reactions to penicillins, cephalosporins, or other allergens. if an allergic reaction occurs, nafcillin should be discontinued and appropriate therapy instituted. clostridium difficile associated diarrhea (cdad) has been reported with use of nearly all antibacterial agents, including nafcillin for injection, and may range in severity from mild diarrhea to fatal colitis. treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of c. difficile . c. difficile produces toxins a and b which contribute to the development of cdad. hypertoxin producing strains
of c. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. cdad must be considered in all patients who present with diarrhea following antibiotic use. careful medical history is necessary since cdad has been reported to occur over two months after the administration of antibacterial agents. if cdad is suspected or confirmed, ongoing antibiotic use not directed against c. difficile may need to be discontinued. appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of c. difficile , and surgical evaluation should be instituted as clinically indicated.

General Precautions:

General nafcillin should generally not be administered to patients with a history of sensitivity to any penicillin. penicillin should be used with caution in individuals with histories of significant allergies and/or asthma. whenever allergic reactions occur, penicillin should be withdrawn unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to penicillin therapy. the use of antibiotics may result in overgrowth of nonsusceptible organisms. if new infections due to bacteria or fungi occur, the drug should be discontinued and appropriate measures taken. the liver/biliary tract is the primary route of nafcillin clearance. caution should be exercised when patients with concomitant hepatic insufficiency and renal dysfunction are treated with nafcillin. prescribing nafcillin for injection in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and incr
eases the risk of the development of drug-resistant bacteria.

Dosage and Administration:

Dosage and administration nafcillin for injection, usp is available for intramuscular and intravenous use. the usual intravenous dosage for adults is 500 mg every 4 hours. for severe infections, 1 gram every 4 hours is recommended. administer slowly over at least 30 to 60 minutes to minimize the risk of vein irritation and extravasation. recommended dosage for nafcillin for injection, usp drug adults infants and children < 40 kg (88 lbs) other recommendations nafcillin 500 mg im every 4 to 6 hours iv every 4 hours 25 mg/kg im twice daily neonates 10 mg/kg im twice daily nafcillin 1 gram im or iv every 4 hours (severe infections) bacteriologic studies to determine the causative organisms and their susceptibility to nafcillin should always be performed. duration of therapy varies with the type and severity of infection as well as the overall condition of the patient; therefore, it should be determined by the clinical and bacteriological response of the patient. in severe staphylococcal i
nfections, therapy with nafcillin should be continued for at least 14 days. the treatment of endocarditis and osteomyelitis may require a longer duration of therapy. no dosage alterations are necessary for patients with renal dysfunction, including those on hemodialysis. hemodialysis does not accelerate nafcillin clearance from the blood. with intravenous administration, particularly in elderly patients, care should be taken because of the possibility of thrombophlebitis. parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. do not add supplementary medication to nafcillin.

Contraindications:

Contraindications a history of a hypersensitivity (anaphylactic) reaction to any penicillin is a contraindication.

Adverse Reactions:

Adverse reactions body as a whole the reported incidence of allergic reactions to penicillin ranges from 0.7 to 10 percent (see warnings ). sensitization is usually the result of treatment, but some individuals have had immediate reactions to penicillin when first treated. in such cases, it is thought that the patients may have had prior exposure to the drug via trace amounts present in milk or vaccines. two types of allergic reactions to penicillins are noted clinically, immediate and delayed. immediate reactions usually occur within 20 minutes of administration and range in severity from urticaria and pruritus to angioedema, laryngospasm, bronchospasm, hypotension, vascular collapse, and death. such immediate anaphylactic reactions are very rare (see warnings ) and usually occur after parenteral therapy but have occurred in patients receiving oral therapy. another type of immediate reaction, an accelerated reaction, may occur between 20 minutes and 48 hours after administration and m
ay include urticaria, pruritus, and fever. although laryngeal edema, laryngospasm, and hypotension occasionally occur, fatality is uncommon. delayed allergic reactions to penicillin therapy usually occur after 48 hours and sometimes as late as 2 to 4 weeks after initiation of therapy. manifestations of this type of reaction include serum sickness-like symptoms (i.e., fever, malaise, urticaria, myalgia, arthralgia, abdominal pain) and various skin rashes. nausea, vomiting, diarrhea, stomatitis, black or hairy tongue, and other symptoms of gastrointestinal irritation may occur, especially during oral penicillin therapy. local reactions pain, swelling, inflammation, phlebitis, thrombophlebitis, and occasional skin sloughing at the injection site have occurred with intravenous administration of nafcillin (see dosage and administration ). severe tissue necrosis with sloughing secondary to subcutaneous extravasation of nafcillin has been reported. nervous system reactions neurotoxic reactions similar to those observed with penicillin g could occur with large intravenous or intraventricular doses of nafcillin especially in patients with concomitant hepatic insufficiency and renal dysfunction (see precautions ). urogenital reactions renal tubular damage and interstitial nephritis have been associated with the administration of nafcillin. manifestations of this reaction may include rash, fever, eosinophilia, hematuria, proteinuria, and renal insufficiency. hepatic reactions elevation of liver transaminases and/or cholestasis may occur, especially with administration of high doses of nafcillin. gastrointestinal reactions pseudomembranous colitis has been reported with the use of nafcillin. the onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment (see warnings ). metabolic reactions agranulocytosis, neutropenia, and bone marrow depression have been associated with the use of nafcillin. to report suspected adverse reactions, contact athenex pharmaceutical division, llc. at 1-855-273-0154 or fda at 1-800-fda-1088 or www.fda.gov/medwatch .

Drug Interactions:

Drug interactions tetracycline, a bacteriostatic antibiotic, may antagonize the bactericidal effect of penicillin, and concurrent use of these drugs should be avoided. nafcillin in high dosage regimens, i.e., 2 grams every 4 hours, has been reported to decrease the effects of warfarin. when nafcillin and warfarin are used concomitantly, the prothrombin time should be closely monitored and the dose of warfarin adjusted as necessary. this effect may persist for up to 30 days after nafcillin has been discontinued. nafcillin when administered concomitantly with cyclosporine has been reported to result in subtherapeutic cyclosporine levels. the nafcillin-cyclosporine interaction was documented in a patient during two separate courses of therapy. when cyclosporine and nafcillin are used concomitantly in organ transplant patients, the cyclosporine levels should be monitored.

Use in Pregnancy:

Pregnancy teratogenic effects reproduction studies have been performed in the mouse with oral doses up to 20 times the human dose and orally in the rat at doses up to 40 times the human dose and have revealed no evidence of impaired fertility or harm to the rodent fetus due to nafcillin. there are, however, no adequate or well-controlled studies in pregnant women. because animal reproduction studies are not always predictive of human response, nafcillin should be used during pregnancy only if clearly needed.

Pediatric Use:

Pediatric use the liver/biliary tract is the principal route of nafcillin elimination. because of immature hepatic and renal function in pediatric patients, nafcillin excretion may be impaired. safety and effectiveness in pediatric patients have not been established for the use of intravenous nafcillin. safety and effectiveness in pediatric patients have been established for the use of intramuscular nafcillin.

Geriatric Use:

Geriatric use clinical studies of nafcillin for injection did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. nafcillin for injection contains 66 mg (2.9 meq) of sodium per gram. at the usual recommended doses, patients would receive between 132 and 396 mg/day (5.8 and 17.4 meq) of sodium. the geriatric population may respond with a blunted natriuresis to salt loading. this may be clinically important with regard to such diseases as congestive heart failure.

Overdosage:

Overdosage neurotoxic reactions similar to those observed with penicillin g may arise with intravenous doses of nafcillin especially in patients with concomitant hepatic insufficiency and renal dysfunction (see precautions ). in the case of overdosage, discontinue nafcillin, treat symptomatically and institute supportive measures as required. hemodialysis does not increase the rate of clearance of nafcillin from the blood.

Description:

Description nafcillin for injection, usp is semisynthetic penicillin derived from the penicillin nucleus, 6-aminopenicillanic acid. the chemical name of nafcillin sodium is monosodium (2s,5r,6r)-6-(2-ethoxy-1-naphthamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0] heptane-2-carboxylate monohydrate. it is resistant to inactivation by the enzyme penicillinase (beta-lactamase). the structural formula of nafcillin sodium is as follows: nafcillin for injection, usp for the intramuscular or intravenous route of administration, contains nafcillin sodium as a sterile white to off-white crystalline dry powder for reconstitution. the reconstituted solution is a clear and colorless solution. the ph of the reconstituted solution is 6 to 8.5. nafcillin for injection, usp contains nafcillin sodium as the monohydrate equivalent to 1 gram or 2 grams of nafcillin per vial and is buffered with approximately 38 mg sodium citrate per gram. the sodium content is about 66 mg [2.9 meq] per gram nafcillin. structural formula

Clinical Pharmacology:

Clinical pharmacology in a study of five healthy adults administered a single 500 mg dose of nafcillin by intravenous injection over seven minutes, the mean plasma concentration of the drug was approximately 30 mcg/ml at 5 minutes after injection. the mean area under the plasma concentration-versus-time curve (auc) for nafcillin in this study was 18.06 mcg•h/ml. the serum half-life of nafcillin administered by the intravenous route ranged from 33 to 61 minutes as measured in three separate studies. in contrast to the other penicillinase-resistant penicillins, only about 30% of nafcillin is excreted as unchanged drug in the urine of normal volunteers, and most within the first six hours. nafcillin is primarily eliminated by nonrenal routes, namely hepatic inactivation and excretion in the bile. nafcillin binds to serum proteins, mainly albumin. the degree of protein binding reported for nafcillin is 89.9 ± 1.5%. reported values vary with the method of study and the investigator.
the concurrent administration of probenecid with nafcillin increases and prolongs plasma concentrations of nafcillin. probenecid significantly reduces the total body clearance of nafcillin with renal clearance being decreased to a greater extent than nonrenal clearance. the penicillinase-resistant penicillins are widely distributed in various body fluids, including bile, pleural, amniotic and synovial fluids. with normal doses insignificant concentrations are found in the aqueous humor of the eye. high nafcillin csf levels have been obtained in the presence of inflamed meninges. renal failure does not appreciably affect the serum half-life of nafcillin; therefore, no modification of the usual nafcillin dosage is necessary in renal failure with or without hemodialysis. hemodialysis does not accelerate the rate of clearance of nafcillin from the blood. a study which assessed the effects of cirrhosis and extrahepatic biliary obstruction in man demonstrated that the plasma clearance of nafcillin was significantly decreased in patients with hepatic dysfunction. in these patients with cirrhosis and extrahepatic obstruction, nafcillin excretion in the urine was significantly increased from about 30 to 50% of the administered dose, suggesting that renal disease superimposed on hepatic disease could further decrease nafcillin clearance.

Pharmacokinetics:

Pharmacokinetics intramuscular injections of nafcillin sodium, 1 gram produced peak serum levels in 0.5 to 1 hour of 7.61 mcg/ml. the degree of protein binding reported has been 89.9 +/-1.5%. with normal doses nafcillin is found in therapeutic concentrations in the pleural, bile, and amniotic fluids. insignificant concentrations are found in the cerebrospinal fluid and aqueous humor. blood concentrations may be tripled by the concurrent use of probenecid. clinical studies with nafcillin sodium in infants under three days of age and prematures have revealed higher blood levels and slower rates of urinary excretion than in older children and adults. a high concentration of nafcillin sodium is excreted via the bile. about 30% of an intramuscular dose is excreted in the urine.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility no long-term animal studies have been conducted with these drugs. studies on reproduction (nafcillin) in rats and mice reveal no fetal or maternal abnormalities before conception and continuously through weaning (one generation).

How Supplied:

How supplied nafcillin for injection, usp is supplied as follows: ndc nafcillin for injection, usp package factor 70860-116-26 1 gram per vial 10 vials per carton 70860-117-26 2 grams per vial 10 vials per carton nafcillin for injection, usp contains nafcillin sodium as the monohydrate equivalent to 1 gram or 2 grams of nafcillin per vial. storage conditions store dry powder at 20° to 25°c (68° to 77°f). [see usp controlled room temperature.] sterile, nonpyrogenic, preservative-free. the container closure is not made with natural rubber latex. athenex mfd. for athenex schaumburg, il 60173 (usa) made in romania ©2022 athenex. revised: december 2022 p303pus3/02a

Information for Patients:

Information for patients patients should be counseled that antibacterial drugs including nafcillin for injection should only be used to treat bacterial infections. they do not treat viral infections (e.g., the common cold). when nafcillin for injection is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by nafcillin for injection or other antibacterial drugs in the future. diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued. sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late
as two or more months after having taken the last dose of the antibiotic. if this occurs, patients should contact their physician as soon as possible.

Package Label Principal Display Panel:

Package label – principal display panel – vial label ndc 70860-116-41 nafcillin for injection, usp 1 gram per vial rx only buffered, sterile for intravenous or intramuscular use package label – principal display panel – vial label

Package label – principal display panel – vial label ndc 70860-117-41 nafcillin for injection, usp 2 grams per vial rx only buffered, sterile for intravenous or intramuscular use package label – principal display panel – vial label


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