Clindamycin Phosphate Injection, Solution
FDA Label NDC 0338-9549

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)]

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)].

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 WarningBoxed_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.

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.

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.

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.

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.

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.

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.

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)].

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.

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

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:

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.

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.

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

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

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.

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.

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

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].

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.

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.

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

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

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.

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.

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.

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

• Clostridium difficile Associated Diarrhea [see Warnings and Precautions (5.1)]
• Anaphylactic and Severe Hypersensitivity Reactions [see Warnings and Precautions (5.2)]

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

Antibiotic-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)].

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.

Erythromycin

•  Antagonism has been demonstrated between clindamycin and erythromycin in vitro. Because of possible clinical significance, the two drugs should not be administered concurrently.

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.

Clindamycin is present 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. There is no information on the effects of clindamycin on milk production. 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.

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.

Clindamycin may cause intestinal flora alteration. Advise a woman to monitor the breastfed infant for diarrhea, candidiasis (thrush, diaper rash) and bloody stools.

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.

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)].

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.

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 (Image 01)

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.

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

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

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

Serum levels 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.

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

Biologically inactive clindamycin phosphate disappears rapidly from the serum; the average elimination half-life is 6 minutes; however, the serum elimination half-life of active clindamycin is about 3 hours in adults and 2 ½ hours in pediatric patients.

Patients with Renal 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, 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.

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

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.

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

When available, the clinical microbiology laboratory should provide cumulative reports of in vitro susceptibility test results for antimicrobial drugs used in local hospitals and practice areas as periodic reports that describe the susceptibility profile of nosocomial and community-acquired pathogens. These reports should aid in the selection of an appropriate antibacterial drug for treatment.

•  Dilution Techniques
•  Quantitative methods are used to determine antimicrobial MICs. These MICs provide estimates of the susceptibility of bacteria to antimicrobial compounds. The MICs should be determined using a standardized test method^2,3 (broth and/or agar). The MIC values should be interpreted according to criteria provided in Table 3.
•  Diffusion Techniques
•  Quantitative methods that require the measurement of zone diameters can also provide reproducible estimates of the susceptibility of bacteria to antimicrobial compounds. The zone size should be determined using a standardized test method^2,5. This procedure uses paper disks impregnated with 2 mcg of clindamycin to test the susceptibility of bacteria to clindamycin. The disk diffusion breakpoints are provided in Table 3.
•  Anaerobic Techniques
•  For anaerobic bacteria, the susceptibility to clindamycin can be determined by a standardized test method^2,4. The MIC values obtained should be interpreted according to the criteria provided in Table 3.

Table 3. Susceptibility Test Interpretive Criteria for Clindamycin

Pathogen	Susceptibility Interpretive Criteria
	Minimum Inhibitory Concentrations (mcg/mL)			Disk Diffusion (zone diameters in mm)
	S	I	R	S	I	R
Staphylococcus spp.	≤ 0.5	1–2	≥4	≥21	15–20	≤14
Streptococcus pneumoniae and other Streptococcus spp.	≤0.25	0.5	≥1	≥19	16–18	≤15
Anaerobic Bacteria	≤2	4	≥8	NA	NA	NA

•  NA = not applicable

A report of Susceptible (S) indicates that the antimicrobial drug is likely to inhibit growth of the pathogen if the antimicrobial drug reaches the concentration usually achievable at the site of infection. A report of Intermediate (I) indicates that the result should be considered equivocal, and, if the microorganism is not fully susceptible to alternative, clinically feasible drugs, the test should be repeated. This category implies possible clinical applicability in body sites where the drug is physiologically concentrated or in situations where high dosage of drug can be used. This category also provides a buffer zone that prevents small, uncontrolled technical factors from causing major discrepancies in interpretation. A report of Resistant (R) indicates that the antimicrobial drug is not likely to inhibit growth of the pathogen if the antimicrobial drug reaches the concentration usually achievable at the infection site; other therapy should be selected.

Standardized susceptibility test procedures require the use of laboratory controls to monitor and ensure the accuracy and precision of the supplies and reagents used in the assay, and the techniques of the individuals performing the test^2,3,4,5. Standard clindamycin powder should provide the following range of MIC values noted in Table 4. For the diffusion technique using the 2 mcg clindamycin disk, the criteria in Table 3 should be achieved.

•  NA = not applicable
•  ATCC^® is a registered trademark of the American Type Culture Collection

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.

•  1. Smith RB, Phillips JP: Evaluation of CLEOCIN HCl and CLEOCIN Phosphate in an Aged Population. Upjohn TR 8147-82-9122-021, December 1982.
•  2.CLSI. Performance Standards for Antimicrobial Susceptibility Testing: 27^th ed. CLSI supplement M100. Wayne, PA: Clinical and Laboratory Standards Institute; 2017.
•  3.CLSI. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically; Approved Standard - Tenth Edition. CLSI document M07-A10. Wayne, PA: Clinical and Laboratory Standards Institute; 2015.
•  4.CLSI. Methods for Antimicrobial Susceptibility Testing of Anaerobic Bacteria; Approved Standard-Eighth Edition. CLSI document M11-A8. Wayne, PA: Clinical and Laboratory Standards Institute; 2012.
•  5.CLSI. Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard - Twelfth Edition. CLSI document M02-A12. Wayne, PA: Clinical and Laboratory Standards Institute; 2015.

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:

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.

• 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.

07-19-78-320

Clindamycin In Sodium Chloride Representative Container Label Ndc 0338-9545-50 (Image 02)

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 0338-9545-24 1 Of 3 (Image 03)

Clindamycin In Sodium Chloride Representative Carton Label Ndc 0338-9545-24 2 Of 3 (Image 04)

Clindamycin In Sodium Chloride Representative Carton Label Ndc 0338-9545-24 3 Of 3 (Image 05)

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.

Clindamycin In Sodium Chloride Representative Container Label Ndc 0338-9549-50 (Image 06)

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 0338-9549-24 1 Of 3 (Image 07)

Clindamycin In Sodium Chloride Representative Carton Label Ndc 0338-9549-24 2 Of 3 (Image 08)

Clindamycin In Sodium Chloride Representative Carton Label Ndc 0338-9549-24 3 Of 3 (Image 09)

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.

Clindamycin In Sodium Chloride Representative Container Label Ndc 0338-9553-50 (Image 10)

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 0338-9553-24 1 Of 3 (Image 11)



Clindamycin In Sodium Chloride Representative Carton Label Ndc 0338-9553-24 2 Of 3 (Image 12)



Clindamycin In Sodium Chloride Representative Carton Label Ndc 0338-9553-24 3 Of 3 (Image 13)

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.