Bicillin L-a

Penicillin G Benzathine


Pfizer Laboratories Div Pfizer Inc
Human Prescription Drug
NDC 60793-702
Bicillin L-a also known as Penicillin G Benzathine is a human prescription drug labeled by 'Pfizer Laboratories Div Pfizer Inc'. National Drug Code (NDC) number for Bicillin L-a is 60793-702. This drug is available in dosage form of Injection, Suspension. The names of the active, medicinal ingredients in Bicillin L-a drug includes Penicillin G Benzathine - 2400000 [iU]/4mL . The currest status of Bicillin L-a drug is Active.

Drug Information:

Drug NDC: 60793-702
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: Bicillin L-a
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: Penicillin G Benzathine
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Injection, Suspension
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:PENICILLIN G BENZATHINE - 2400000 [iU]/4mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:INTRAMUSCULAR
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: NDA
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: 27 Jun, 1952
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: NDA050141
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:Pfizer Laboratories Div Pfizer Inc
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:731564
731566
731567
731568
731570
731571
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:RIT82F58GK
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
60793-702-1010 SYRINGE in 1 PACKAGE (60793-702-10) / 4 mL in 1 SYRINGE (60793-702-04)27 Jun, 1952N/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:

Bicillin l-a penicillin g benzathine penicillin g benzathine penicillin g lecithin, soybean carboxymethylcellulose sodium, unspecified povidone, unspecified methylparaben propylparaben sodium citrate, unspecified form water bicillin l-a penicillin g benzathine penicillin g benzathine penicillin g lecithin, soybean carboxymethylcellulose sodium, unspecified povidone, unspecified methylparaben propylparaben sodium citrate, unspecified form water bicillin l-a penicillin g benzathine penicillin g benzathine penicillin g lecithin, soybean carboxymethylcellulose sodium, unspecified povidone, unspecified methylparaben propylparaben sodium citrate, unspecified form water

Drug Interactions:

Drug interactions tetracycline, a bacteriostatic antibiotic, may antagonize the bactericidal effect of penicillin, and concurrent use of these drugs should be avoided. concurrent administration of penicillin and probenecid increases and prolongs serum penicillin levels by decreasing the apparent volume of distribution and slowing the rate of excretion by competitively inhibiting renal tubular secretion of penicillin.

Boxed Warning:

Warning not for intravenous use. do not inject intravenously or admix with other intravenous solutions. there have been reports of inadvertent intravenous administration of penicillin g benzathine which has been associated with cardiorespiratory arrest and death. prior to administration of this drug, carefully read the warnings , adverse reactions , and dosage and administration sections of the labeling.

Warning not for intravenous use. do not inject intravenously or admix with other intravenous solutions. there have been reports of inadvertent intravenous administration of penicillin g benzathine which has been associated with cardiorespiratory arrest and death. prior to administration of this drug, carefully read the warnings , adverse reactions , and dosage and administration sections of the labeling.

Indications and Usage:

Indications and usage to reduce the development of drug-resistant bacteria and maintain the effectiveness of bicillin l-a and other antibacterial drugs, bicillin l-a should be used only to treat or prevent infections that are proven or strongly suspected to be caused by 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. intramuscular penicillin g benzathine is indicated in the treatment of infections due to penicillin-g-sensitive microorganisms that are susceptible to the low and very prolonged serum levels common to this particular dosage form. therapy should be guided by bacteriological studies (including sensitivity tests) and by clinical response. the following infections will usually respond to adequate dosage of intramuscular penicillin g benzathine: mild-to-mode
rate infections of the upper-respiratory tract due to susceptible streptococci. venereal infections —syphilis, yaws, bejel, and pinta. medical conditions in which penicillin g benzathine therapy is indicated as prophylaxis: rheumatic fever and/or chorea —prophylaxis with penicillin g benzathine has proven effective in preventing recurrence of these conditions. it has also been used as follow-up prophylactic therapy for rheumatic heart disease and acute glomerulonephritis.

Warnings:

Warnings warning not for intravenous use. do not inject intravenously or admix with other intravenous solutions. there have been reports of inadvertent intravenous administration of penicillin g benzathine which has been associated with cardiorespiratory arrest and death. prior to administration of this drug, carefully read the warnings , adverse reactions , and dosage and administration sections of the labeling. penicillin g benzathine should only be prescribed for the indications listed in this insert. anaphylaxis 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. there have been reports of individuals with a history of penicillin hypersensitivity who have experienced severe reactions when treated with cephalosporins. before initiating therapy with bicill
in l-a, careful inquiry should be made concerning previous hypersensitivity reactions to penicillins, cephalosporins, or other allergens. if an allergic reaction occurs, bicillin l-a should be discontinued and appropriate therapy instituted. serious anaphylactic reactions require immediate emergency treatment with epinephrine. oxygen, intravenous steroids and airway management, including intubation, should also be administered as indicated. severe cutaneous adverse reactions severe cutaneous adverse reactions (scar), such as stevens-johnson syndrome (sjs), toxic epidermal necrolysis (ten), drug reaction with eosinophilia and systemic symptoms (dress), and acute generalized exanthematous pustulosis (agep) have been reported in patients taking penicillin g (the active moiety in bicillin l-a). when scar is suspected, bicillin l-a should be discontinued immediately and an alternative treatment should be considered. clostridioides difficile associated diarrhea clostridioides difficile associated-diarrhea (cdad) has been reported with use of nearly all antibacterial agents, including bicillin l-a, 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 antibacterial 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. method of administration do not inject into or near an artery or nerve. see administration instructions below. injection into or near a nerve may result in permanent neurological damage. inadvertent intravascular administration, including inadvertent direct intra-arterial injection or injection immediately adjacent to arteries, of bicillin l-a and other penicillin preparations has resulted in severe neurovascular damage, including transverse myelitis with permanent paralysis, gangrene requiring amputation of digits and more proximal portions of extremities, and necrosis and sloughing at and surrounding the injection site consistent with the diagnosis of nicolau syndrome. such severe effects have been reported following injections into the buttock, thigh, and deltoid areas. other serious complications of suspected intravascular administration which have been reported include immediate pallor, mottling, or cyanosis of the extremity both distal and proximal to the injection site, followed by bleb formation; severe edema requiring anterior and/or posterior compartment fasciotomy in the lower extremity. the above-described severe effects and complications have most often occurred in infants and small children. prompt consultation with an appropriate specialist is indicated if any evidence of compromise of the blood supply occurs at, proximal to, or distal to the site of injection. 1–9 (see precautions , and dosage and administration sections.) for deep intramuscular injection only. there have been reports of inadvertent intravenous administration of penicillin g benzathine which has been associated with cardiorespiratory arrest and death. therefore, do not inject intravenously or admix with other intravenous solutions. (see dosage and administration section.) administer by deep intramuscular injection only in the upper, outer quadrant of the buttock (dorsogluteal) or the ventrogluteal site. quadriceps femoris fibrosis and atrophy have been reported following repeated intramuscular injections of penicillin preparations into the anterolateral thigh. because of these adverse effects and the vascularity of this region, administration in the anterolateral thigh is not recommended.

General Precautions:

General prescribing bicillin l-a in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of a development of drug-resistant bacteria. penicillin should be used with caution in individuals with histories of significant allergies and/or asthma. care should be taken to avoid intravenous or intra-arterial administration, or injection into or near major peripheral nerves or blood vessels, since such injection may produce neurovascular damage. (see warnings , and dosage and administration sections.) prolonged use of antibiotics may promote the overgrowth of nonsusceptible organisms, including fungi. should superinfection occur, appropriate measures should be taken. bicillin l-a contains approximately 0.11 meq of sodium per 600,000 units of penicillin g (approximately 2.59 mg of sodium per 600,000 units of penicillin g).

Dosage and Administration:

Dosage and administration streptococcal (group a) upper respiratory infections (for example, pharyngitis) adults—a single injection of 1,200,000 units; older pediatric patients—a single injection of 900,000 units; infants and pediatric patients under 60 lbs.—300,000 to 600,000 units. syphilis primary, secondary, and latent—2,400,000 units (1 dose). late (tertiary and neurosyphilis)—2,400,000 units at 7-day intervals for three doses. congenital—under 2 years of age: 50,000 units/kg/body weight; ages 2 to 12 years: adjust dosage based on adult dosage schedule. yaws, bejel, and pinta —1,200,000 units (1 injection). prophylaxis —for rheumatic fever and glomerulonephritis. following an acute attack, penicillin g benzathine (parenteral) may be given in doses of 1,200,000 units once a month or 600,000 units every 2 weeks. method of administration bicillin l-a is intended for intramuscular injection only. do not inject into or near an artery or nerve, or
intravenously or admix with other intravenous solutions. (see warnings section.) administer by deep intramuscular injection in the upper, outer quadrant of the buttock (dorsogluteal) or the ventrogluteal site. in neonates, infants and small children, the midlateral aspect of the thigh may be preferable. administration in the anterolateral thigh is not recommended due to the adverse effects observed (see warnings section), and vascularity of this region. when doses are repeated, vary the injection site. because of the high concentration of suspended material in this product, the needle may be blocked if the injection is not made at a slow, steady rate. parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit.

Contraindications:

Contraindications a history of a previous hypersensitivity reaction to any of the penicillins is a contraindication.

Adverse Reactions:

Adverse reactions as with other penicillins, untoward reactions of the sensitivity phenomena are likely to occur, particularly in individuals who have previously demonstrated hypersensitivity to penicillins or in those with a history of allergy, asthma, hay fever, or urticaria. as with other treatments for syphilis, the jarisch-herxheimer reaction has been reported. the following adverse reactions have been reported with bicillin l-a during post-marketing experience: skin and appendages: stevens-johnson syndrome (sjs) and drug reaction with eosinophilia and systemic symptoms (dress). (see warnings .) the following have been reported with parenteral penicillin g (the active moiety in bicillin l-a): general: hypersensitivity reactions including the following: skin eruptions (maculopapular to exfoliative dermatitis), urticaria, laryngeal edema, fever, eosinophilia; other serum sickness-like reactions (including chills, fever, edema, arthralgia, and prostration); and anaphylaxis including
shock and death: severe cutaneous adverse reactions (scar), such as toxic epidermal necrolysis (ten) and acute generalized exanthematous pustulosis (agep). (see warnings .) note: urticaria, other skin rashes, and serum sickness-like reactions may be controlled with antihistamines and, if necessary, systemic corticosteroids. whenever such reactions occur, penicillin g should be discontinued unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to therapy with penicillin g. serious anaphylactic reactions require immediate emergency treatment with epinephrine. oxygen, intravenous steroids, and airway management, including intubation, should also be administered as indicated. gastrointestinal: pseudomembranous colitis. onset of pseudomembranous colitis symptoms may occur during or after antibacterial treatment. (see warnings section.) hematologic: hemolytic anemia, leukopenia, thrombocytopenia. neurologic: neuropathy. urogenital: nephropathy. the following adverse events have been temporally associated with parenteral administration of penicillin g benzathine (a component of bicillin l-a): body as a whole: hypersensitivity reactions including allergic vasculitis, pruritus, fatigue, asthenia, and pain; aggravation of existing disorder; headache, nicolau syndrome. cardiovascular: cardiac arrest; hypotension; tachycardia; palpitations; pulmonary hypertension; pulmonary embolism; vasodilation; vasovagal reaction; cerebrovascular accident; syncope. gastrointestinal: nausea, vomiting; blood in stool; intestinal necrosis. hemic and lymphatic: lymphadenopathy. injection site: injection site reactions including pain, inflammation, lump, abscess, necrosis, edema, hemorrhage, cellulitis, hypersensitivity, atrophy, ecchymosis, and skin ulcer. neurovascular reactions including warmth, vasospasm, pallor, mottling, gangrene, numbness of the extremities, cyanosis of the extremities, and neurovascular damage. metabolic: elevated bun, creatinine, and sgot. musculoskeletal: joint disorder; periostitis; exacerbation of arthritis; myoglobinuria; rhabdomyolysis. nervous system: nervousness; tremors; dizziness; somnolence; confusion; anxiety; euphoria; transverse myelitis; seizures; coma. a syndrome manifested by a variety of cns symptoms such as severe agitation with confusion, visual and auditory hallucinations, and a fear of impending death (hoigne's syndrome), has been reported after administration of penicillin g procaine and, less commonly, after injection of the combination of penicillin g benzathine and penicillin g procaine. other symptoms associated with this syndrome, such as psychosis, seizures, dizziness, tinnitus, cyanosis, palpitations, tachycardia, and/or abnormal perception in taste, also may occur. respiratory: hypoxia; apnea; dyspnea. skin: diaphoresis. special senses: blurred vision; blindness. urogenital: neurogenic bladder; hematuria; proteinuria; renal failure; impotence; priapism.

Drug Interactions:

Drug interactions tetracycline, a bacteriostatic antibiotic, may antagonize the bactericidal effect of penicillin, and concurrent use of these drugs should be avoided. concurrent administration of penicillin and probenecid increases and prolongs serum penicillin levels by decreasing the apparent volume of distribution and slowing the rate of excretion by competitively inhibiting renal tubular secretion of penicillin.

Use in Pregnancy:

Pregnancy teratogenic effects pregnancy reproduction studies performed in the mouse, rat, and rabbit have revealed no evidence of impaired fertility or harm to the fetus due to penicillin g. human experience with the penicillins during pregnancy has not shown any positive evidence of adverse effects on the fetus. there are, however, no adequate and well-controlled studies in pregnant women showing conclusively that harmful effects of these drugs on the fetus can be excluded. because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Pediatric Use:

Pediatric use (see indications and usage and dosage and administration sections.)

Geriatric Use:

Geriatric use clinical studies of penicillin g benzathine 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. this drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. (see clinical pharmacology .) because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

Overdosage:

Overdosage penicillin in overdosage has the potential to cause neuromuscular hyperirritability or convulsive seizures.

Description:

Description bicillin l-a (penicillin g benzathine injectable suspension) is available for deep intramuscular injection. penicillin g benzathine is prepared by the reaction of dibenzylethylene diamine with two molecules of penicillin g. it is chemically designated as (2 s , 5 r , 6 r )-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid compound with n,n' - dibenzylethylenediamine (2:1), tetrahydrate. it occurs as a white, crystalline powder and is very slightly soluble in water and sparingly soluble in alcohol. its chemical structure is as follows: bicillin l-a contains penicillin g benzathine in aqueous suspension with sodium citrate buffer and, as w/v, approximately 0.65% sodium citrate, 0.59% povidone, 0.54% carboxymethylcellulose sodium, 0.53% lecithin, 0.12% methylparaben, and 0.013% propylparaben. bicillin l-a contains approximately 0.11 meq of sodium per 600,000 units of penicillin g (approximately 2.59 mg of sodium per 600,000 units of penicillin g). bicillin l-a suspension in the disposable-syringe formulation is viscous and opaque. it is available in a 1 ml, 2 ml, and 4 ml sizes containing the equivalent of 600,000 (actual volume of 1.17 ml contains 620,100), 1,200,000 (actual volume of 2.34 ml contains 1,240,200), and 2,400,000 (actual volume of 4.67 ml contains 2,475,100) units respectively of penicillin g as the benzathine salt. read contraindications, warnings, precautions, and dosage and administration sections prior to use. chemical structure

Clinical Pharmacology:

Clinical pharmacology general penicillin g benzathine has an extremely low solubility and, thus, the drug is slowly released from intramuscular injection sites. the drug is hydrolyzed to penicillin g. this combination of hydrolysis and slow absorption results in blood serum levels much lower but much more prolonged than other parenteral penicillins. intramuscular administration of 300,000 units of penicillin g benzathine in adults results in blood levels of 0.03 to 0.05 units per ml, which are maintained for 4 to 5 days. similar blood levels may persist for 10 days following administration of 600,000 units and for 14 days following administration of 1,200,000 units. blood concentrations of 0.003 units per ml may still be detectable 4 weeks following administration of 1,200,000 units. approximately 60% of penicillin g is bound to serum protein. the drug is distributed throughout the body tissues in widely varying amounts. highest levels are found in the kidneys with lesser amounts in th
e liver, skin, and intestines. penicillin g penetrates into all other tissues and the spinal fluid to a lesser degree. with normal kidney function, the drug is excreted rapidly by tubular excretion. in neonates and young infants and in individuals with impaired kidney function, excretion is considerably delayed. microbiology mechanism of action penicillin g exerts a bactericidal action against penicillin-susceptible microorganisms during the stage of active multiplication. it acts through the inhibition of biosynthesis of cell-wall peptidoglycan, rendering the cell wall osmotically unstable. resistance penicillin is not active against penicillinase-producing bacteria or against organisms resistant to beta-lactams because of alterations in the penicillin-binding proteins. resistance to penicillin g has not been reported in streptococcus pyogenes . antimicrobial activity penicillin has been shown to be active against most isolates of the following bacteria, both in vitro and in clinical infections as described in the indications and usage section. gram-positive bacteria beta-hemolytic streptococci (groups a, b, c, g, h, l and m). other microorganisms treponema pallidum treponema carateum susceptibility testing for specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by fda for this drug, please see: https://www.fda.gov/stic.

Mechanism of Action:

Mechanism of action penicillin g exerts a bactericidal action against penicillin-susceptible microorganisms during the stage of active multiplication. it acts through the inhibition of biosynthesis of cell-wall peptidoglycan, rendering the cell wall osmotically unstable.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility no long-term animal studies have been conducted with this drug.

How Supplied:

How supplied bicillin l-a (penicillin g benzathine injectable suspension) is supplied in packages of 10 disposable syringes as follows: 1 ml size, containing 600,000 units per syringe, (21 gauge, thin-wall 1-inch needle for pediatric use), with 0.11 meq of sodium per 600,000 units of penicillin g (2.59 mg of sodium per 600,000 units of penicillin g), ndc 60793-700-10. 2 ml size, containing 1,200,000 units per syringe, (21 gauge, thin-wall 1-1/2-inch needle), with 0.22 meq of sodium per 1,200,000 units of penicillin g (5.17 mg of sodium per 1,200,000 units of penicillin g), ndc 60793-701-10. 4 ml size, containing 2,400,000 units per syringe (18 gauge, × 1–1/2-inch needle), with 0.45 meq of sodium per 2,400,000 units of penicillin g (10.32 mg of sodium per 2,400,000 units of penicillin g), ndc 60793-702-10. store in a refrigerator, 2° to 8°c (36° to 46°f). keep from freezing.

Information for Patients:

Information for patients 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. patients should be counseled that antibacterial drugs including bicillin l-a should only be used to treat bacterial infections. they do not treat viral infections (e.g., the common cold). when bicillin l-a 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 b
acteria will develop resistance and will not be treatable by bicillin l-a or other antibacterial drugs in the future.

Package Label Principal Display Panel:

Principal display panel - 1 ml syringe label ndc 60793-700-01 bicillin ® l-a (penicillin g benzathine injectable suspension) 600,000 units per 1 ml for deep intramuscular injection only warning: fatal if given by other routes distributed by pfizer inc new york, ny 10017 principal display panel - 1 ml syringe label

Principal display panel - 1 ml syringe package ndc 60793-700-10 contains 10 of ndc 60793-700-01 ten syringes (1 ml size) bicillin ® l-a (penicillin g benzathine injectable suspension) 600,000 units per 1 ml for pediatric use for deep intramuscular injection only warning: fatal if given by other routes before injecting, see package insert for administration instructions. pfizer injectables rx only principal display panel - 1 ml syringe package

Principal display panel - 2 ml syringe label ndc 60793-701-02 bicillin ® l-a (penicillin g benzathine injectable suspension) 1,200,000 units per 2 ml for deep intramuscular injection only warning: fatal if given by other routes distributed by pfizer inc new york, ny 10017 principal display panel - 2 ml syringe label

Principal display panel - 2 ml syringe package ndc 60793-701-10 contains 10 of ndc 60793-701-02 ten syringes (2 ml size) bicillin ® l-a (penicillin g benzathine injectable suspension) 1,200,000 units per 2 ml for deep intramuscular injection only warning: fatal if given by other routes before injecting, see package insert for administration instructions. pfizer injectables rx only principal display panel - 2 ml syringe package

Principal display panel - 4 ml syringe label ndc 60793-702-04 bicillin ® l-a (penicillin g benzathine injectable suspension) 2,400,000 units per 4 ml for deep intramuscular injection only warning: fatal if given by other routes distributed by pfizer inc new york, ny 10017 principal display panel - 4 ml syringe label

Principal display panel - 4 ml syringe package ndc 60793-702-10 contains 10 of ndc 60793-702-04 ten syringes (4 ml size) bicillin ® l-a (penicillin g benzathine injectable suspension) 2,400,000 units per 4 ml disposable syringe for deep intramuscular injection only warning: fatal if given by other routes before injecting, see package insert for administration instructions. pfizer injectables rx only principal display panel - 4 ml syringe package


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.