CLINDAMYCIN PHOSPHATE injection, solution

clindamycin phosphate by

Drug Labeling and Warnings

clindamycin phosphate by is a Prescription medication manufactured, distributed, or labeled by Baxter Healthcare Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: CLOSTRIDIUM DIFFICILE-ASSOCIATED DIARRHEA (CDAD) and COLITIS

    Clostridium difficile-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including Clindamycin in 0.9% Sodium Chloride 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.

    Because Clindamycin in 0.9% Sodium Chloride Injection therapy has been associated with severe colitis which may end fatally, it should be reserved for serious infections where less toxic antimicrobial agents are inappropriate [see Indications and Usage (1)]. It should not be used in patients with nonbacterial infections such as most upper respiratory tract infections. 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 antibacterial use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibacterial treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated. [see Warnings and Precautions (5.1)]

  • 1 INDICATIONS AND USAGE

    1.1 Infections Due to Susceptible Anaerobic Bacteria

    Clindamycin in 0.9% Sodium Chloride Injection is indicated for the treatment of serious infections caused by susceptible anaerobic bacteria [see Indications and Usage (1.3 - 1.7)].

    1.2 Infections Due to Susceptible Strains of Streptococci, Pneumococci and Staphylococci

    Clindamycin in 0.9% Sodium Chloride Injection is indicated for the treatment of serious infections due to susceptible strains of streptococci, pneumococci, and staphylococci. Its use should be reserved for penicillin-allergic patients or other patients for whom, in the judgment of the physician, a penicillin is inappropriate. Because of the risk of antibacterial-associated pseudomembranous colitis, [see Boxed Warning], before selecting clindamycin the physician should consider the nature of the infection and the suitability of less toxic alternatives (e.g., erythromycin).

    Bacteriologic studies should be performed to determine the causative organisms and their susceptibility to clindamycin.

    Indicated surgical procedures should be performed in conjunction with antibacterial therapy.

    1.3 Lower Respiratory Tract Infections

    Clindamycin in 0.9% Sodium Chloride Injection is indicated in the treatment of serious lower respiratory tract infections including pneumonia, empyema, and lung abscess caused by susceptible strains of anaerobes, Streptococcus pneumoniae, other streptococci (except E. faecalis), and Staphylococcus aureus.

    1.4 Skin and Skin Structure Infections

    Clindamycin in 0.9% Sodium Chloride Injection is indicated in the treatment of serious skin and skin structure infections caused by susceptible strains of Streptococcus pyogenes, Staphylococcus aureus, and anaerobes.

    1.5 Gynecological Infections

    Clindamycin in 0.9% Sodium Chloride Injection is indicated in the treatment of serious gynecological infections including endometritis, nongonococcal tubo-ovarian abscess, pelvic cellulitis, and postsurgical vaginal cuff infection caused by susceptible anaerobes.

    1.6 Intra-abdominal Infections

    Clindamycin in 0.9% Sodium Chloride Injection is indicated in the treatment of serious intra-abdominal infections including peritonitis and intra-abdominal abscess caused by susceptible anaerobic organisms.

    1.7 Septicemia

    Clindamycin in 0.9% Sodium Chloride Injection is indicated in the treatment of serious septicemia caused by susceptible strains of Staphylococcus aureus, streptococci (except Enterococcus faecalis), and susceptible anaerobes.

    1.8 Bone and Joint Infections

    Clindamycin in 0.9% Sodium Chloride Injection is indicated in the treatment of serious bone and joint infections including acute hematogenous osteomyelitis caused by susceptible strains of Staphylococcus aureus and as adjunctive therapy in the surgical treatment of chronic bone and joint infections due to susceptible organisms.

    1.9 Limitations of Use

    Since clindamycin does not diffuse adequately into the cerebrospinal fluid, Clindamycin in 0.9% Sodium Chloride Injection should not be used in the treatment of meningitis [see Clinical Pharmacology (12.3)].

    1.10 Usage

    To reduce the development of drug-resistant bacteria and maintain the effectiveness of Clindamycin in 0.9% Sodium Chloride Injection and other antibacterial drugs, Clindamycin in 0.9% Sodium Chloride 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.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Discontinuation Instructions

    Discontinue Clindamycin in 0.9% Sodium Chloride Injection if diarrhea occurs during therapy [see Boxed Warning].

    2.2 Recommended Adult Dosage

    The recommended dosing regimen for Clindamycin in 0.9% Sodium Chloride Injection is 600-1200 mg/day in 2, 3, or 4 equal doses by intravenous infusion for serious infections due to aerobic gram-positive cocci and the more susceptible anaerobes (NOT generally including Bacteroides fragilis, Peptococcus species and Clostridium species other than Clostridium perfringens).

    For more severe infections, particularly those due to proven or suspected Bacteroides fragilis, Peptococcus species, or Clostridium species other than Clostridium perfringens, the recommended dosing regimen is 1200-2700 mg/day in 2, 3, or 4 equal doses by intravenous infusion.

    In life-threatening situations, these doses may be increased. Doses of as much as 4800 mg daily have been given intravenously to adults [see Dosage and Administration (2.4)].

    Alternatively, drug may be administered in the form of a single rapid infusion of the first dose followed by continuous intravenous infusion as follows:

    Table 1: Infusion Rates for the Administration of Clindamycin Injection by Single Rapid Infuion followed by Continuous Intravenous Infusion

    To maintain serum
    clindamycin levels

    Rapid infusion rate

    Maintenance infusion rate

    Above 4 mcg/mL

    10 mg/min for 30 min

    0.75 mg/min

    Above 5 mcg/mL

    15 mg/min for 30 min

    1.00 mg/min

    Above 6 mcg/mL

    20 mg/min for 30 min

    1.25 mg/min

    2.3 Dosage in Pediatric Patients (1 Month of Age to 16 Years)

    The recommended dosing regimen for pediatric patients is 20 to 40 mg/kg/day in 3 or 4 equal doses by intravenous infusion. The higher doses would be used for more severe infections. As an alternative to dosing on a body weight basis, pediatric patients may be dosed on the basis of square meters body surface: 350 mg/m2/day for serious infections and 450 mg/m2/day for more severe infections.

    Parenteral therapy may be changed to oral clindamycin palmitate hydrochloride powder for oral solution or clindamycin hydrochloride capsules when the condition warrants and at the discretion of the physician.

    In cases of β-hemolytic streptococcal infections, treatment should be continued for at least 10 days.

    2.4 Dosage in Pediatric Patients (Neonates Less than 1 Month)

    The recommended dosing regimen for neonates is 15 to 20 mg/kg/day in 3 to 4 equal doses by intravenous infusion. The lower dosage may be adequate for small prematures.

    2.5 Intravenous Infusion Rates

    Infusion rates should NOT exceed 30 mg per minute. The usual infusion rates are as follows:

    Dose

    Time

    300 mg

    10 min

    600 mg

    20 min

    900 mg

    30 min

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    2.6 Directions for Use of Clindamycin in 0.9% Sodium Chloride Injection in GALAXY Plastic Container

    Premixed Clindamycin in 0.9% Sodium Chloride Injection is for intravenous infusion using sterile equipment. Check for minute leaks prior to use by squeezing bag firmly. If leaks are found, discard solution as sterility may be impaired. Do NOT add supplementary medication. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. Do NOT use unless solution is clear and seal is intact.

    Do NOT use plastic containers in series connections. Such use could result in air embolism due to residual air being drawn from the primary container before administration of the fluid from the secondary container is complete.

    Preparation for Administration:

    • 1. Suspend container from eyelet support.
    • 2. Remove protector from outlet port at bottom of container.
    • 3. Attach administration set. Refer to complete directions accompanying set.
  • 3 DOSAGE FORMS AND STRENGTHS

    Injection: Sterile, clear and colorless solution available in three strengths:

    • 300 mg/50 mL (6 mg/mL): Each 50 mL single-dose GALAXY container contains 300 mg clindamycin (as clindamycin phosphate, USP) in 0.9% sodium chloride.
    • 600 mg/50 mL (12 mg/mL): Each 50 mL single-dose GALAXY container contains 600 mg clindamycin (as clindamycin phosphate, USP) in 0.9% sodium chloride.
    • 900 mg/50 mL (18 mg/mL): Each 50 mL single-dose GALAXY container contains 900 mg clindamycin (as clindamycin phosphate, USP) in 0.9% sodium chloride.
  • 4 CONTRAINDICATIONS

    Clindamycin in 0.9 % Sodium Chloride Injection is contraindicated in individuals with a history of hypersensitivity to preparations containing clindamycin or lincomycin.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Clostridium difficile Associated Diarrhea

    Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including Clindamycin in 0.9% Sodium Chloride 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 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 antibacterial use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibacterial treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated [see Boxed Warning].

    5.2 Anaphylactic and Severe Hypersensitivity Reactions

    Anaphylactic shock and anaphylactic reactions have been reported [see Adverse Reactions (6)]. Severe hypersensitivity reactions, including severe skin reactions such as toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), and Stevens-Johnson syndrome (SJS), some with fatal outcome, have been reported [see Adverse Reactions (6)].

    In case of such an anaphylactic or severe hypersensitivity reaction, discontinue treatment permanently and institute appropriate therapy.

    A careful inquiry should be made concerning previous sensitivities to drugs and other allergens.

    5.3 Diarrhea in Elderly Patients with Associated Severe Illness

    Elderly patients with associated severe illness may have a greater risk of developing adverse reactions from diarrhea. When clindamycin is indicated in these patients, they should be carefully monitored for change in bowel frequency.

    5.4 Use in Patients with Gastrointestinal Disease

    Clindamycin in 0.9% Sodium Chloride Injection products should be avoided in individuals with a history of gastrointestinal disease, particularly colitis.

    5.5 Use in Atopic Individuals

    Clindamycin in 0.9% Sodium Chloride Injection should be avoided in atopic individuals.

    5.6 Laboratory Tests: Monitoring to Assess Safety

    During prolonged therapy periodic liver and kidney function tests and blood counts should be performed.

    Clindamycin dosage modification may not be necessary in patients with renal disease. In patients with moderate to severe liver disease, prolongation of clindamycin half-life has been found. However, it was postulated from studies that when given every eight hours, accumulation should rarely occur. Therefore, dosage modification in patients with liver disease may not be necessary. However, periodic liver enzyme determinations should be made when treating patients with severe liver disease.

    5.7 Overgrowth of Nonsusceptible Organisms

    The use of Clindamycin in 0.9% Sodium Chloride Injection may result in overgrowth of nonsusceptible organisms-particularly yeasts. If such infections occur, appropriate measures should be taken as indicated by the clinical situation.

    5.8 Development of Drug-Resistant Bacteria

    Prescribing Clindamycin in 0.9% Sodium Chloride 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 increases the risk of the development of drug-resistant bacteria.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions to clindamycin are described below and elsewhere in the labeling:

    The following adverse reactions associated with the use of clindamycin were identified in clinical trials or postmarketing reports. Because these reactions were reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably, or to establish a causal relationship to drug exposure.

    Infections and Infestations

    Clostridium difficile colitis

    Gastrointestinal

    Antibacterial-associated colitis [see Warnings and Precautions (5.1)], pseudomembranous colitis, abdominal pain, nausea, and vomiting. The onset of pseudomembranous colitis symptoms may occur during or after antibacterial treatment [see Warnings and Precautions (5.1)]. An unpleasant or metallic taste has been reported after intravenous administration of the higher doses of clindamycin phosphate.

    Hypersensitivity Reactions

    Maculopapular rash and urticaria have been observed during drug therapy. Generalized mild to moderate morbilliform-like skin rashes are the most frequently reported of all adverse reactions.

    Severe skin reactions such as Toxic Epidermal Necrolysis, some with fatal outcome, have been reported [see Warnings and Precautions (5.2)]. Cases of Acute Generalized Exanthematous Pustulosis (AGEP), erythema multiforme, some resembling Stevens-Johnson syndrome, have been associated with clindamycin. Anaphylactic shock, anaphylactic reaction and hypersensitivity have also been reported [see Warnings and Precautions (5.2)].

    Skin and Mucous Membranes

    Pruritus, vaginitis, angioedema and rare instances of exfoliative dermatitis have been reported [see Warnings and Precautions (5.2)].

    Liver

    Jaundice and abnormalities in liver function tests have been observed during clindamycin therapy.

    Renal

    Renal dysfunction as evidenced by azotemia, oliguria, and/or proteinuria has been observed.

    Hematopoietic

    Transient neutropenia (leukopenia) and eosinophilia have been reported. Reports of agranulocytosis and thrombocytopenia have been made.

    Immune System

    Drug reaction with eosinophilia and systemic symptoms (DRESS) cases have been reported.

    Local Reactions

    Thrombophlebitis has been reported after intravenous infusion. Avoid prolonged use of indwelling intravenous catheters.

    Musculoskeletal

    Polyarthritis cases have been reported.

    Cardiovascular

    Cardiopulmonary arrest and hypotension have been reported following too rapid intravenous administration [see Dosage and Administration (2)].

  • 7 DRUG INTERACTIONS

    7.1 Neuromuscular Blocking Agents

    Clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. Therefore, it should be avoided in patients receiving such agents.

    7.2 Inhibitors of CYP3A4 and CYP3A5

    Inhibitors of CYP3A4 and/or CYP3A5 may increase plasma concentrations of clindamycin [see Clinical Pharmacology (12.3)]. Monitor for adverse reactions when strong CYP3A4 and/or CYP3A5 inhibitors are coadministered with clindamycin.

    7.3 Inhibitors of CYP3A4 and CYP3A5

    Inducers of CYP3A4 and/or CYP3A5 may reduce plasma concentrations of clindamycin. In the presence of strong CYP3A4 and/or CYP3A5 inducers such as rifampicin, monitor for loss of effectiveness.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    In limited published clinical trials with pregnant women, the systemic administration of clindamycin during the second and third trimesters, has not been associated with an increased frequency of major birth defects.

    The limited published data on use of clindamycin in pregnant women with exposure during the first trimester are insufficient to inform a drug-associated risk of pregnancy-related adverse outcomes [see Data]. In animal reproduction studies, no evidence of any adverse developmental outcomes was observed when oral or subcutaneous doses of clindamycin were administered to pregnant rats and mice during organogenesis at doses half to twice the highest clinically relevant dose based on body surface area comparison [see Data]. The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.

    Data

    Human Data

    In limited published trials in pregnant women administered clindamycin during the first trimester of pregnancy, there was no difference in the rate of major birth defects reported among in utero exposed infants compared to unexposed infants. From these observational data, it is not possible to draw any conclusions on the rate of specific major birth defects associated with clindamycin. These data cannot definitely establish or exclude any clindamycin-associated risk during pregnancy.

    Animal Data

    Reproduction studies performed during organogenesis (gestational days 6-15) in pregnant rats and mice that were administered oral doses of clindamycin up to 600 mg/kg/day (twice or equivalent to the highest recommended adult human dose based on a body surface area comparison, respectively) or subcutaneous doses of clindamycin up to 250 mg/kg/day (equivalent to or half the highest recommended adult human dose based on a body surface area comparison, respectively) revealed no evidence of teratogenicity.

    8.2 Lactation

    Risk Summary

    Clindamycin has been reported to appear in breast milk in the range of 0.7 to 3.8 mcg/mL at dosages of 150 mg orally to 600 mg intravenously. Clindamycin has the potential to cause adverse effects on the breastfed infant’s gastrointestinal flora.

    The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for clindamycin and any potential adverse effects on the breast-fed child from clindamycin or from the underlying maternal condition.

    Clinical Considerations

    If oral or intravenous clindamycin is required by a nursing mother, it is not a reason to discontinue breastfeeding, but an alternate drug may be preferred. Monitor the infant for possible adverse effects on the gastrointestinal flora, such as diarrhea, candidiasis (thrush, diaper rash) or blood in the stool indicating possible antibacterial-associated colitis.

    8.4 Pediatric Use

    When Clindamycin in 0.9% Sodium Chloride Injection is administered to the pediatric population (birth to 16 years) appropriate dosing and monitoring of organ system functions is desirable.

    The potential for the toxic effect in the pediatric population from chemicals that may leach from the single dose premixed intravenous preparation in plastic has not been evaluated.

    8.5 Geriatric Use

    Clinical studies of clindamycin did not include sufficient numbers of patients age 65 and over to determine whether they respond differently from younger patients. However, other reported clinical experience indicates that antibacterial-associated colitis and diarrhea (due to Clostridium difficile) seen in association with most antibacterial drugs occur more frequently in the elderly (>60 years) and may be more severe. These patients should be carefully monitored for the development of diarrhea.

    Pharmacokinetic studies with clindamycin have shown no clinically important differences between young and elderly subjects with normal hepatic function and normal (age-adjusted) renal function after oral or intravenous administration [see Clinical Pharmacology (12.3)].

  • 10 OVERDOSAGE

    Significant mortality was observed in mice at an intravenous dose of 855 mg/kg (~3 times the human dose based on body surface area) and in rats at an oral or subcutaneous dose of approximately 2618 mg/kg (~18 times the human dose based on body surface area). In the mice, convulsions and depression were observed and in rats depression was observed prior to death.

    Hemodialysis and peritoneal dialysis are not effective in removing clindamycin from the serum.

  • 11 DESCRIPTION

    Clindamycin is a lincosamide antibacterial and a semisynthetic drug produced by a 7(S) chloro substitution of the 7(R) hydroxyl group of the parent compound lincomycin.

    The chemical name of clindamycin phosphate is L-threo-α-D-galacto-Octopyranoside, methyl-7-chloro-6,7,8-trideoxy-6-[[(1-methyl-4-propyl-2-pyrrolidinyl)carbonyl]amino]‑1-thio-, 2-(dihydrogen phosphate), (2S-trans)-.

    The molecular formula is C18H34CIN2O8PS and the molecular weight is 504.96.

    The structural formula is represented below:

    Clindamycin Structural Formula

    Clindamycin in 0.9% Sodium Chloride Injection is a clear, cloroless and sterile solution for intravenous infusion. Each 50 mL Clindamycin in 0.9% Sodium Chloride Injection, 300 mg/50 mL, 600 mg/50 mL, and 900 mg/50 mL, contains 300 mg, 600 mg or 900 mg clindamycin, respectively (as clindamycin phosphate, USP), 450 mg of sodium chloride USP, 2 mg of edetate disodium dihydrate USP, and water for Injection USP. The pH is adjusted with sodium hydroxide and /or hydrochloric acid. Clindamycin in 0.9% Sodium Chloride Injection is filled in GALAXY plastic container fabricated from a specially designed multilayer plastic, PL 2501. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period. The suitability of the plastic has been confirmed in tests in animals according to the USP biological tests for plastic containers, as well as by tissue culture toxicity studies.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Clindamycin is an antibacterial drug [see Microbiology (12.4)].

    12.3 Pharmacokinetics

    Biologically inactive clindamycin phosphate is converted to active clindamycin. By the end of short-term intravenous infusion, peak serum concentrations of active clindamycin are reached.

    After intramuscular injection of clindamycin phosphate, peak concentrations of active clindamycin are reached within 3 hours in adults and 1 hour in pediatric patients. Serum concentration-time curves may be constructed from intravenous peak serum concentrations as given in Table 2 by application of elimination half-lives described in the elimination section below.

    Serum concentrations of clindamycin can be maintained above the in vitro minimum inhibitory concentrations for most indicated organisms by administration of clindamycin phosphate every 8 to 12 hours in adults and every 6 to 8 hours in pediatric patients, or by continuous intravenous infusion. An equilibrium state is reached by the third dose.

    Serum assays for active clindamycin require an inhibitor to prevent in vitro hydrolysis of clindamycin phosphate.

    Table 2. Average Peak and Trough Serum Concentrations of Active Clindamycin After Dosing with Clindamycin Phosphate
  • * Data in this group from patients being treated for infection.
    		•

    Dosage Regimen

    Peak

    mcg/mL

    Trough

    mcg/mL

    Healthy Adult Males

    (Post equilibrium)

    •   600 mg IV in 30 min q6h

    10.9

    2.0
    •   600 mg IV in 30 min q8h

    10.8

    1.1
    •   900 mg IV in 30 min q8h

    14.1

    1.7

    Pediatric Patients (first dose)*

    •   5–7 mg/kg IV in 1 hour

    10

    Distribution

    No significant concentrations of clindamycin are attained in the cerebrospinal fluid even in the presence of inflamed meninges.

    Elimination

    Clindamycin is metabolized predominantly by CYP3A4, and to a lesser extent by CYP3A5, to the major metabolite clindamycin sulfoxide and minor metabolite N-desmethylclindamycin. Biologically inactive clindamycin phosphate disappears from the serum with 6 minutes of the average elimination half-life; however, the average serum elimination half-life of active clindamycin is about 3 hours in adults and 2.5 hours in pediatric patients.

    Specific Populations

    Patients with Renal/Hepatic Impairment

    The elimination half-life of clindamycin is increased slightly in patients with markedly reduced renal or hepatic function. Hemodialysis and peritoneal dialysis are not effective in removing clindamycin from the serum. Dosage schedules need not be modified in the presence of mild or moderate renal or hepatic disease.

    Geriatric Patients

    Pharmacokinetic studies in elderly volunteers (61-79 years) and younger adults (18-39 years) indicate that age alone does not alter clindamycin pharmacokinetics (clearance, elimination half-life, volume of distribution, and area under the serum concentration-time curve) after intravenous administration of clindamycin phosphate. After oral administration of clindamycin hydrochloride, the average elimination half-life is increased to approximately 4.0 hours (range 3.4-5.1 h) in the elderly, compared to 3.2 hours (range 2.1-4.2 h) in younger adults. The extent of absorption, however, is not different between age groups and no dosage alteration is necessary for the elderly with normal hepatic function and normal (age-adjusted) renal function1.

    Drug Interaction Studies

    In vitro studies indicate that clindamycin does not inhibit CYP1A2, CYP2C9, CYP2C19, CYP2E1 or CYP2D6 and only moderately inhibits CYP3A4.

    12.4 Microbiology

    Mechanism of Action

    Clindamycin inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S subunit of the ribosome. Clindamycin is bacteriostatic.

    Resistance

    Resistance to clindamycin is most often caused by modification of specific bases of the 23S ribosomal RNA. Cross-resistance between clindamycin and lincomycin is complete. Because the binding sites for these antibacterial drugs overlap, cross-resistance is sometimes observed among lincosamides, macrolides and streptogramin B. Macrolide-inducible resistance to clindamycin occurs in some isolates of macrolide-resistant bacteria. Macrolide-resistant isolates of staphylococci and beta-hemolytic streptococci should be screened for induction of clindamycin resistance using the D-zone test.

    Antimicrobial Activity

    Clindamycin has been shown to be active against most of the isolates of the following microorganisms, both in vitro and in clinical infections [see Indications and Usage (1)].

    •   Aerobic bacteria
      •   Gram-positive bacteria
    •   Staphylococcus aureus (methicillin-susceptible strains)
      Streptococcus pneumoniae (penicillin-susceptible strains)
      Streptococcus pyogenes
    •   Anaerobic bacteria
    •   Gram-positive bacteria
    •   Clostridium perfringens
      Peptostreptococcus anaerobius
    •   Gram-negative bacteria
    •   Fusobacterium necrophorum
      Fusobacterium nucleatum
      Prevotella melaninogenica

    The following in vitro data are available, but their clinical significance is unknown. At least 90 percent of the following bacteria exhibit an in vitro minimum inhibitory concentration (MIC) less than or equal to the susceptible breakpoint for clindamycin against isolates of similar genus or organism group. However, the efficacy of clindamycin in treating clinical infections caused by these bacteria has not been established in adequate and well-controlled clinical trials.

    •   Aerobic bacteria
    •   Gram-positive bacteria
    •   Staphylococcus epidermidis (methicillin-susceptible strains)
      Streptococcus agalactiae
      Streptococcus anginosus
      Streptococcus mitis
      Streptococcus oralis
    •   Anaerobic bacteria
    •   Gram-positive bacteria
    •   Actinomyces israelii
      Clostridium clostridioforme
      Eggerthella lenta
      Finegoldia (Peptostreptococcus) magna
      Micromonas (Peptostreptococcus) micros
      Propionibacterium acnes
    •   Gram-negative bacteria
    •   Prevotella bivia
      Prevotella intermedia

    Susceptibility Test Methods

    For specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by FDA for this drug, please see: http://www.fda.gov/STIC.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long term studies in animals have not been performed with clindamycin to evaluate carcinogenic potential. Genotoxicity tests performed included a rat micronucleus test and an Ames Salmonella reversion test. Both tests were negative.

    Fertility studies in rats treated orally with up to 300 mg/kg/day (approximately 1.1 times the highest recommended adult human dose based on mg/m2) revealed no effects on fertility or mating ability.

  • 15 REFERENCES

    •   1. Smith RB, Phillips JP: Evaluation of CLEOCIN HCl and CLEOCIN Phosphate in an Aged Population. Upjohn TR 8147-82-9122-021, December 1982.
  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Clindamycin in 0.9% Sodium Chloride Injection for intravenous infusion. Each 50 mL of Clindamycin in 0.9% Sodium Chloride Injection, 300 mg/50 mL, 600 mg/50 mL, and 900 mg/50 mL, contains 300 mg, 600 mg or 900 mg clindamycin, respectively (as clindamycin phosphate, USP). Clindamycin in 0.9% Sodium Chloride Injection in single-dose GALAXY containers is available as follows:

    2G3455

    Twenty-four (24)-300 mg/50 mL containers

    NDC: 0338-9545-24

    2G3456

    Twenty-four (24)-600 mg/50 mL containers

    NDC: 0338-9549-24

    2G3457

    Twenty-four (24)-900 mg/50 mL containers

    NDC: 0338-9553-24

    Exposure of pharmaceutical products, including Clindamycin in 0.9 % Sodium Chloride, to heat should be minimized. It is recommended that GALAXY plastic containers be stored at 20°C to 25°C (68°F to 77°F) excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature]. Avoid temperatures above 30°C.

  • 17 PATIENT COUNSELING INFORMATION

    • Counsel patients that antibacterial drugs including Clindamycin in 0.9% Sodium Chloride Injection should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When Clindamycin in 0.9% Sodium Chloride Injection is prescribed to treat a bacterial infection, inform patient 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 Clindamycin in 0.9% Sodium Chloride Injection or other antibacterial drugs in the future.
    • Counsel patients that diarrhea is a common problem caused by antibacterial drugs which usually ends when the antibacterial is discontinued. Sometimes after starting treatment with antibacterial drugs, 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 antibacterial drugs. If this occurs, contact physician as soon as possible [see Warnings and Precautions (5.4)].
    • Lactation: Advise a woman to monitor the breastfed infant for diarrhea and bloody stools [see Use in Specific Populations (8.2)].

    Baxter and Galaxy are registered trademarks of Baxter International Inc.

    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    Made in USA.

    07-19-01-299

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    Clindamycin in Sodium Chloride Representative Container Label NDC: <a href=/NDC/0338-9545-50>0338-9545-50</a>

    Container Label

    NDC: 0338-9545-50
    Clindamycin in 0.9% Sodium Chloride Injection

    300 mg per 50 mL
    (6 mg / mL)

    50 mL Single Dose GALAXY Container
    Code 2G3455

    Discard unused portion
    Sterile Nonpyrogenic

    For Intravenous Infusion Only

    Cautions: Do not add supplementary medication. Must not be used in series
    connections. Check for minute leaks and solution clarity.

    Each 50 mL contains: Clindamycin phosphate, USP equivalent to 300 mg
    clindamycin, 450 mg sodium chloride, USP, 2 mg edetate disodium dihydrate,
    USP, and Water for Injection, USP. pH may have been adjusted with sodium
    hydroxide and/or hydrochloric acid.

    Dosage: See prescribing information.

    Rx only
    Store at 20°C to 25°C (68°F to 77°F)[see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    PL 2501 Plastic

    BAXTER Logo

    Baxter and Galaxy are registered trademarks of Baxter International Inc.
    Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Made in USA

    07-34-00-0002

    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9545-24>0338-9545-24</a> 1 of 3
    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9545-24>0338-9545-24</a> 2 of 3
    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9545-24>0338-9545-24</a> 3 of 3

    Carton Label

    GALAXY Container PL 2501 Plastic

    BAXTER Logo

    Baxter and Galaxy are registered trademarks of Baxter International Inc.
    Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Made in USA

    Clindamycin in 0.9% Sodium Chloride Injection
    Rx only
    NDC: 0338-9545-24

    300 mg per 50 mL (6 mg / mL)
    Code 2G3455

    Contains 12 - 50 mL Single Dose Containers
    Store at 20°C to 25°C (68°F to 77°F) [see USP Controlled
    Room Temperature]. Avoid temperatures above 30°C.

    FOR BAR CODE POSITION ONLY
    (01) XXXXXXXXXXXX

    For Intravenous Infusion Only
    Sterile Nonpyrogenic

    Each 50 mL contains: Clindamycin phosphate, USP equivalent to 300 mg clindamycin, 450 mg sodium
    chloride, USP, 2 mg edetate disodium dihydrate, USP, and Water for Injection, USP. pH may have been adjusted with
    sodium hydroxide and/or hydrochloric acid.
    Dosage: See prescribing information.
    Cautions: Do not add supplementary medication. Must not be used in series connections. Check for minute
    leaks and solution clarity.

    Representative Serialized Label 0338-9545-24

    Serialized Carton

    Clindamycin in 0.9% Sodium Chloride
    Injection 300mg/50mL
    Code 2G3455 NDC: 0338-9545-24

    Store at 20°C to 25°C (68°F to 77°F)
    [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    Rx Only
    Baxter Logo
    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    LOT NC123456
    EXP DD MMM YY
    SN 0123456789

    Clindamycin in 0.9% Sodium Chloride
    Injection 300mg/50mL
    Code 2G3455 NDC: 0338-9545-24

    Rx Only
    Baxter Logo
    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    Store at 20°C to 25°C (68°F to 77°F)
    [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    LOT NC123456
    EXP DD MMM YY
    SN 0123456789

    07-06-77-459

    Clindamycin in Sodium Chloride Representative Container Label NDC: <a href=/NDC/0338-9549-50>0338-9549-50</a>

    Container Label

    NDC 0338-9549-50
    Clindamycin in 0.9% Sodium Chloride Injection

    600 mg per 50 mL
    (12 mg / mL)

    50 mL Single Dose GALAXY Container
    Code 2G3456

    Discard unused portion
    Sterile Nonpyrogenic
    For Intravenous Use Only

    Cautions: Do not add supplementary medication. Must not be used in series connections. Check for minute leaks and solution clarity.

    Each 50 mL contains: Clindamycin phosphate, USP equivalent to 600 mg clindamycin, 450 mg sodium chloride, USP, 2 mg edetate disodium dihydrate, USP, and Water for Injection, USP. pH may have been adjusted with sodium hydroxide and/or hydrochloric acid.

    Dosage: See prescribing information.

    Rx only
    Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    PL 2501 Plastic

    BAXTER Logo

    Baxter and Galaxy are registered trademarks of Baxter International Inc.
    Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Made in USA

    07-34-78-381

    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9549-24>0338-9549-24</a> 1 of 3
    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9549-24>0338-9549-24</a> 2 of 3
    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9549-24>0338-9549-24</a> 3 of 3

    Carton Label

    GALAXY Container
    PL 2501 Plastic

    BAXTER Logo

    Baxter and Galaxy are registered trademarks of Baxter International Inc.
    Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Made in USA

    07-04-78-379

    Clindamycin in 0.9% Sodium Chloride Injection
    Rx only
    NDC: 0338-9549-24

    600 mg per 50 mL (12 mg / mL)
    Code 2G3456

    Contains 12 - 50 mL Single Dose Containers
    Store at 20°C to 25°C (68°F to 77°F)[see USP Controlled
    Room Temperature]. Avoid temperatures above 30°C.

    FOR BAR CODE POSITION ONLY
    (01) XXXXXXXXXXXX

    For Intravenous Infusion Only
    Sterile Nonpyrogenic

    Each 50 mL contains: Clindamycin phosphate, USP equivalent to 600 mg clindamycin, 450 mg sodium
    chloride, USP, 2 mg edetate disodium dihydrate, USP, and Water for Injection, USP. pH may have been
    adjusted with sodium hydroxide and/or hydrochloric acid.

    Dosage: See prescribing information.
    Cautions: Do not add supplementary medication. Must not be used in series connections. Check for minute
    leaks and solution clarity.

    Representative Serialized Carton 0338-9549-24

    Serialized Carton

    Clindamycin in 0.9% Sodium Chloride
    Injection 600mg/50mL
    Code 2G3456 NDC: 0338-9549-24

    Store at 20°C to 25°C (68°F to 77°F)
    [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    Rx Only
    Baxter Logo
    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    LOT NC123456
    EXP DD MMM YY
    SN 0123456789

    Clindamycin in 0.9% Sodium Chloride
    Injection 600mg/50mL
    Code 2G3456 NDC: 0338-9549-24

    Rx Only
    Baxter Logo
    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    Store at 20°C to 25°C (68°F to 77°F)
    [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    LOT NC123456
    EXP DD MMM YY
    SN 0123456789

    07-06-77-460

    Clindamycin in Sodium Chloride Representative Container Label NDC: <a href=/NDC/0338-9553-50>0338-9553-50</a>

    Container Label

    NDC: 0338-9553-50
    Clindamycin in 0.9% Sodium Chloride Injection

    900 mg per 50 mL
    (18 mg / mL)

    •   50 mL Single Dose GALAXY Container
      Discard unused portion
      Code 2G3457
      Sterile Nonpyrogenic
      For Intravenous Infusion Only

    Cautions: Do not add supplementary medication. Must not be used in series
    connections. Check for minute leaks and solution clarity.

    Each 50 mL contains: Clindamycin phosphate, USP equivalent to 900 mg
    clindamycin, 450 mg sodium chloride, USP, 2 mg edetate disodium dihydrate,
    USP, and Water for Injection, USP. pH may have been adjusted with sodium
    hydroxide and/or hydrochloric acid.
    Dosage: See prescribing information.

    Rx only
    Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    PL 2501 Plastic

    BAXTER Logo

    Baxter and Galaxy are registered trademarks of Baxter International Inc.
    Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Made in USA

    07-34-78-382

    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9553-24>0338-9553-24</a> 1 of 3
    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9553-24>0338-9553-24</a> 2 of 3
    Clindamycin in Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-9553-24>0338-9553-24</a> 3 of 3

    Carton Label

    GALAXY Container
    PL 2501 Plastic

    BAXTER Logo

    Baxter and Galaxy are registered trademarks of Baxter International Inc.
    Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Made in USA

    07-04-78-380

    Clindamycin in 0.9% Sodium Chloride Injection
    Rx only
    NDC: 0338-9553-24

    900 mg per 50 mL (18 mg / mL)
    Code 2G3457

    Contains 12 - 50 mL Single Dose Containers
    Store at 20°C to 25°C (68°F to 77°F)[see USP Controlled
    Room Temperature]. Avoid temperatures above 30°C.

    FOR BAR CODE POSITION ONLY
    (01) XXXXXXXXXXXX

    For Intravenous Infusion Only
    Sterile Nonpyrogenic

    Each 50 mL contains: Clindamycin phosphate, USP equivalent to 900 mg clindamycin, 450 mg sodium
    chloride, USP, 2 mg edetate disodium dihydrate, USP, and Water for Injection, USP. pH may have been
    adjusted with sodium hydroxide and/or hydrochloric acid.

    Dosage: See prescribing information.

    Caution: Do not add supplementary medication. Must not be used in series connections. Check for minute
    leaks and solution clarity.

    Representative Seriazlized Carton 0338-9553-24

    Serialized Carton

    Clindamycin in 0.9% Sodium Chloride
    Injection 900mg/50mL
    Code 2G3457 NDC: 0338-9553-24

    Store at 20°C to 25°C (68°F to 77°F)
    [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    Rx Only
    Baxter Logo
    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    LOT NC123456
    EXP DD MMM YY
    SN 0123456789

    Clindamycin in 0.9% Sodium Chloride
    Injection 900mg/50mL
    Code 2G3457 NDC: 0338-9553-24

    Rx Only
    Baxter Logo
    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA

    Store at 20°C to 25°C (68°F to 77°F)
    [see USP Controlled Room Temperature].
    Avoid temperatures above 30°C.

    LOT NC123456
    EXP DD MMM YY
    SN 0123456789

    07-06-77-461

  • INGREDIENTS AND APPEARANCE
    CLINDAMYCIN PHOSPHATE 
    clindamycin phosphate injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-9545
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLINDAMYCIN PHOSPHATE (UNII: EH6D7113I8) (CLINDAMYCIN - UNII:3U02EL437C) CLINDAMYCIN PHOSPHATE300 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K) 2.00 mg  in 50 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 9.00 mg  in 50 mL
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-9545-2424 in 1 CARTON04/20/2017
    1NDC: 0338-9545-5050 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20808304/20/2017
    CLINDAMYCIN PHOSPHATE 
    clindamycin phosphate injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-9549
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLINDAMYCIN PHOSPHATE (UNII: EH6D7113I8) (CLINDAMYCIN - UNII:3U02EL437C) CLINDAMYCIN PHOSPHATE600 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K) 2.00 mg  in 50 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 9.00 mg  in 50 mL
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-9549-2424 in 1 CARTON04/20/2017
    1NDC: 0338-9549-5050 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20808304/20/2017
    CLINDAMYCIN PHOSPHATE 
    clindamycin phosphate injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-9553
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLINDAMYCIN PHOSPHATE (UNII: EH6D7113I8) (CLINDAMYCIN - UNII:3U02EL437C) CLINDAMYCIN PHOSPHATE900 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K) 2.00 mg  in 50 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 9.00 mg  in 50 mL
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-9553-2424 in 1 CARTON04/20/2017
    1NDC: 0338-9553-5050 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20808304/20/2017
    Labeler - Baxter Healthcare Corporation (005083209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Baxter Healthcare Corporation194684502ANALYSIS(0338-9545, 0338-9549, 0338-9553) , LABEL(0338-9545, 0338-9549, 0338-9553) , MANUFACTURE(0338-9545, 0338-9549, 0338-9553) , PACK(0338-9545, 0338-9549, 0338-9553) , STERILIZE(0338-9545, 0338-9549, 0338-9553)
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