Label: MARBOQUIN- marbofloxacin tablet

  • NDC Code(s): 17033-125-10, 17033-125-25, 17033-126-10, 17033-126-25, view more
    17033-127-50, 17033-128-50
  • Packager: Dechra Veterinary Products LLC
  • Category: PRESCRIPTION ANIMAL DRUG LABEL

Drug Label Information

Updated September 24, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • SPL UNCLASSIFIED SECTION

    For oral use in dogs and cats only

  • SPL UNCLASSIFIED SECTION

    CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

    Federal law prohibits the extralabel use of this drug in food-producing animals.

  • DESCRIPTION

    DESCRIPTION: Marbofloxacin is a synthetic broad-spectrum antibacterial agent from the fluoroquinolone class of chemotherapeutic agents. Marbofloxacin is the non-proprietary designation for 9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[3,2,1-ij][4,1,2] benzoxadiazine-6-carboxylic acid. The empirical formula is C17H19FN4O4 and the molecular weight is 362.36. The compound is soluble in water; however, solubility decreases in alkaline conditions. The N-octanol/water partition coefficient (Kow) is 0.835 measured at pH 7 and 25°C.

    Figure 1: Chemical structure of marbofloxacin

    Figure 1

  • CLINICAL PHARMACOLOGY

    CLINICAL PHARMACOLOGY: Marbofloxacin is rapidly and almost completely absorbed from the gastrointestinal tract following oral administration to fasted animals. Divalent cations are generally known to diminish the absorption of fluoroquinolones. The effects of concomitant feeding on the absorption of marbofloxacin have not been determined. (See Drug Interactions.) In the dog, approximately 40% of an oral dose of marbofloxacin is excreted unchanged in the urine1. Excretion in the feces, also as unchanged drug, is the other major route of elimination in dogs. Ten to 15% of marbofloxacin is metabolized by the liver in dogs.

    In vitro plasma protein binding of marbofloxacin in dogs was 9.1% and in cats was 7.3%. In the cat, approximately 70% of an oral dose is excreted in the urine as marbofloxacin and metabolites with approximately 85% of the excreted material as unchanged drug. Pharmacokinetic parameters related to intravenous dosing were estimated in a study of 6 healthy adult beagle dogs, and are summarized in Table 1. The absolute bioavailability following dosing of oral tablets to the same animals was 94%.

    Marbofloxacin plasma concentrations were determined over time in healthy adult beagle dogs (6 dogs per dosage group) following single oral doses of 1.25 mg/lb or 2.5 mg/lb. Absorption of orally administered marbofloxacin increases proportionally over the dose range of 1.25 to 2.5 mg/lb. Marbofloxacin plasma concentrations were determined over time in 7 healthy adult male cats following a single oral dose of 2.5 mg/lb. Plasma pharmacokinetic parameters following oral dosing of dogs and cats are summarized in Figures 2 and 3 and in Table 2. Based on the terminal elimination half-life and the dosing interval, steady-state levels are reached after the third dose and are expected to be approximately 25% greater in dogs and 35% greater in cats than those achieved after a single dose. Marbofloxacin is widely distributed in canine tissues. Tissue concentrations of marbofloxacin were determined in healthy male beagle dogs (4 dogs per time period) at 2, 18 and 24 hours after a single oral dose (1.25 or 2.5 mg/lb) and are summarized in Tables 3a and 3b.

    Table 1: Mean pharmacokinetic parameters following intravenous administration of marbofloxacin to 6 adult beagle dogs at a dosage of 2.5 mg/lb.
    ParameterEstimate ± SD*
    n=6
    *
    SD = standard deviation
    Total body clearance, (mL/h∙kg)94 ± 8
    Volume of distribution at steady-state, Vss,(L/kg)1.19 ± 0.08
    AUC0-inf (μg∙h/mL)59 ± 5
    Terminal plasma elimination half-life, t1/2(h)9.5 ± 0.7
    Table 2: Mean pharmacokinetic parameters following oral administration of marbofloxacin tablets to adult beagle dogs at a nominal dosage of 1.25 mg/lb or 2.5 mg/lb and to cats at 2.5 mg/lb.*
    ParameterDog Estimate ± SD
    (1.25 mg/lb)
    n=6
    Dog Estimate ± SD
    (2.5 mg/lb)
    n=6
    Cat Estimate ± SD
    (2.5 mg/lb)
    n=7
    *
    mean actual dosages administered to dogs were 1.22 mg/lb and 2.56 mg/lb, respectively, and the mean actual dosage administered to cats was 2.82 mg/lb.
    SD = standard deviation
    Time of maximum concentration, Tmax(h)1.5 ± 0.31.8 ± 0.31.2 ± 0.6
    Maximum concentration, Cmax' (μg/mL)2.0 ± 0.24.2 ± 0.54.8 ± 0.7
    AUC0-inf (μg∙h/mL)31.2 ± 1.664 ± 870 ± 6
    Terminal plasma elimination half-life, t1/2(h)10.7 ± 1.610.9 ± 0.612.7 ± 1.1

    Figure 2: Mean plasma concentrations (μg/mL) following single oral administration of marbofloxacin to adult beagle dogs at dosages of 1.25 mg/lb or 2.5 mg/lb.

    * See Table 4 in Microbiology section for MIC data.

    Figure 2

    Figure 3: Mean plasma concentrations (μg/mL) following single oral administration of marbofloxacin to adult cats at a dosage of 2.5 mg/lb.

    * See Table 5 in Microbiology section for MIC data.

    Figure 3

    Table 3a: Tissue distribution following a single oral administration of marbofloxacin tablets to adult beagle dogs at a dosage of 1.25 mg/lb.
    Marbofloxacin Concentrations
    (μg/g ± SD*)
    Tissue2 hours
    (n=4)
    18 hours
    (n=4)
    24 hours
    (n=4)
    *
    SD = standard deviation
    bladder4.8 ± 1.12.6 ± 1.51.11 ± 0.19
    bone marrow3.1 ± 0.51.5 ± 1.50.7 ± 0.2
    feces15 ± 948 ± 4026 ± 11
    jejunum3.6 ± 0.51.3 ± 1.00.7 ± 0.3
    kidney7.1 ±1.71.4 ± 0.50.9 ± 0.3
    lung3.0 ± 0.50.8 ± 0.20.57 ± 0.19
    lymph node5.5 ± 1.11.3 ± 0.31.0 ± 0.3
    muscle4.1 ± 0.31.0 ± 0.30.7 ± 0.2
    prostate5.6 ± 1.41.8 ± 0.61.1 ± 0.4
    skin1.9 ± 0.60.41 ± 0.130.32 ± 0.08
    Table 3b: Tissue distribution following a single oral administration of marbofloxacin tablets to adult beagle dogs at a dosage of 2.5 mg/lb.
    Marbofloxacin Concentrations
    (μg/g ± SD*)
    Tissue2 hours
    (n=4)
    18 hours
    (n=4)
    24 hours
    (n=4)
    *
    SD = standard deviation
    bladder12 ± 46 ± 71.8 ± 0.4
    bone marrow4.6 ± 1.51.28 ± 0.130.9 ± 0.3
    feces18 ± 352 ± 1747 ± 28
    jejunum7.8 ± 1.12.0 ± 0.31.1 ± 0.3
    kidney12.7 ±1.72.7 ± 0.31.6 ± 0.2
    lung5.48 ± 0.171.45 ± 0.191.0 ± 0.2
    lymph node8.3 ± 0.72.3 ± 0.52.03 ± 0.06
    muscle7.5 ± 0.51.8 ± 0.31.20 ± 0.12
    prostate11 ± 32.7 ± 1.02.0 ± 0.5
    skin3.20 ± 0.330.705 ± 0.0130.46 ± 0.09

    Microbiology: The primary action of fluoroquinolones is to inhibit the bacterial enzyme, DNA gyrase. In susceptible organisms, fluoroquinolones are rapidly bactericidal at relatively low concentrations. Marbofloxacin is bactericidal against a broad range of gram-negative and gram-positive organisms. The minimum inhibitory concentrations (MICs) of pathogens isolated in clinical field studies performed in the United States were determined using National Committee for Clinical Laboratory Standards (NCCLS) standards, and are shown in Tables 4 and 5.

    Table 4: MIC Values* (μg/mL) of marbofloxacin against pathogens isolated from skin, soft tissue and urinary tract infections in dogs enrolled in clinical studies conducted during 1994-1996.
    OrganismNo. of IsolatesMIC50MIC90MIC Range
    *
    The correlation between in vitro susceptibility data (MIC) and clinical response has not been determined.
    MIC50 and MIC90 not calculated due to insufficient number of isolates.
    Staphylococcus intermedius1350.250.250.125 - 2
    Escherichia coli610.030.060.015 - 2
    Proteus mirabilis350.060.1250.03 - 0.25
    Beta-hemolytic Streptococcus, (not Group A or Group B)25120.5 - 16
    Streptococcus, Group D enterococcus16140.008 - 4
    Pasteurella multocida130.0150.06≤0.008 - 0.5
    Staphylococcus aureus120.250.250.25 - 0.5
    Enterococcus faecalis11221 - 4
    Klebsiella pneumoniae110.060.060.01 - 0.06
    Pseudomonas spp.90.06 - 1
    Pseudomonas aeruginosa70.25 - 1
    Table 5: MIC Values* (μg/mL) of marbofloxacin against pathogens isolated from skin and soft tissue infections in cats enrolled in clinical studies conducted in 1995 and 1998.
    OrganismNo. of IsolatesMIC50MIC90MIC Range
    *
    The correlation between in vitro susceptibility data (MIC) and clinical response has not been determined.
    Pasteurella multocida1350.030.06≤0.008 - 0.25
    Beta-hemolytic Streptococcus22110.06 - 1
    Staphylococcus aureus210.250.50.125 - 1
    Corynebacterium spp.140.510.25 - 2
    Staphylococcus intermedius110.250.50.03 - 0.5
    Enterococcus faecalis102.02.01.0 - 2.0
    Escherichia coli100.030.030.015 - 0.03
    Bacillus spp.100.250.250.125 - 0.25
  • VETERINARY INDICATIONS

    INDICATIONS AND USAGE: Marboquin (marbofloxacin) tablets are indicated for the treatment of infections in dogs and cats associated with bacteria susceptible to marbofloxacin.

  • CONTRAINDICATIONS

    CONTRAINDICATIONS: Marbofloxacin and other quinolones have been shown to cause arthropathy in immature animals of most species tested, the dog being particularly sensitive to this side effect. Marbofloxacin is contraindicated in immature dogs during the rapid growth phase (small and medium breeds up to 8 months of age, large breeds up to 12 months of age and giant breeds up to 18 months of age). Marbofloxacin is contraindicated in cats under 12 months of age. Marbofloxacin is contraindicated in dogs and cats known to be hypersensitive to quinolones.

  • WARNINGS

    WARNING: For use in animals only. Keep out of reach of children. Avoid contact with eyes. In case of contact, immediately flush eyes with copious amounts of water for 15 minutes. In case of dermal contact, wash skin with soap and water. Consult a physician if irritation persists following ocular or dermal exposure. Individuals with a history of hypersensitivity to fluoroquinolones should avoid this product. In humans, there is a risk of user photosensitization within a few hours after excessive exposure to quinolones. If excessive accidental exposure occurs, avoid direct sunlight.

  • PRECAUTIONS

    PRECAUTIONS: Quinolones should be used with caution in animals with known or suspected central nervous system (CNS) disorders. In such animals, quinolones have, in rare instances, been associated with CNS stimulation which may lead to convulsive seizures. Quinolones have been shown to produce erosions of cartilage of weight-bearing joints and other signs of arthropathy in immature animals of various species. The use of fluoroquinolones in cats has been reported to adversely affect the retina. Such products should be used with caution in cats. The safety of marbofloxacin in animals used for breeding purposes, pregnant, or lactating has not been demonstrated.

  • ADVERSE REACTIONS

    ADVERSE REACTIONS: The following clinical signs were reported during the course of clinical field studies in dogs receiving marbofloxacin at dosages up to 2.5 mg/lb daily: decreased or loss of appetite (5.4%), decreased activity (4.4%), and vomiting (2.9%). The following signs were reported in less than 1% of cases in dogs: increased thirst, soft stool/diarrhea, behavioral changes, shivering/shaking/tremors, and ataxia. One dog which had a seizure the day before study enrollment experienced a seizure while on marbofloxacin therapy.

    The following clinical signs were reported during clinical field studies in cats receiving 1.25 mg/lb/day: diarrhea (2.1%) and soft stool (1.4%). Vomiting was reported in less than 1% of cases in cats.

    To report suspected adverse events, for technical assistance or to obtain a copy of the SDS, contact Dechra at (866) 933-2472.

    For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or http://www.fda.gov/reportanimalae

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION: The recommended dosage for oral administration to dogs and cats is 1.25 mg marbofloxacin per lb of body weight once daily, but the dosage may be safely increased to 2.5 mg/lb.

    For the treatment of skin and soft tissue infections, Marboquin tablets should be given for 2-3 days beyond the cessation of clinical signs for a maximum of 30 days.

    For the treatment of urinary tract infections, Marboquin tablets should be administered for at least 10 days. If no improvement is noted within 5 days, the diagnosis should be re-evaluated and a different course of therapy considered.

    Drug Interactions: Compounds (e.g., sucralfate, antacids, and mineral supplements) containing divalent and trivalent cations (e.g., iron, aluminum, calcium, magnesium, and zinc) can interfere with the absorption of quinolones which may result in a decrease in product bioavailability. Therefore, the concomitant oral administration of quinolones with foods, supplements, or other preparations containing these compounds should be avoided.

  • SPL UNCLASSIFIED SECTION

    EFFECTIVENESS CONFIRMATION: Clinical effectiveness was confirmed in bacterial skin and soft tissue infections in dogs and cats and urinary tract infections (cystitis) in dogs associated with bacteria susceptible to marbofloxacin. Bacterial pathogens isolated in clinical field studies are provided in the Microbiology section.

  • TARGET ANIMAL SAFETY:

    Dogs: The toxicity of marbofloxacin was assessed in 12- to 14-month-old beagle dogs administered marbofloxacin at 2.5, 7.5 and 12.5 mg/lb/day for 42 days. Vomiting, reddened skin (usually involving the ears) and reddened mucous membranes were occasionally observed in all groups, including controls, but were noted most frequently in the 12.5 mg/lb group. Decreased food consumption and weight loss were significant in the 7.5 mg/lb and 12.5 mg/lb groups. No clinical lameness was noted in any of the treated animals. Minimal to slight lesions in the articular cartilage were observed in 1/8 placebo-treated animals and in 3/8 animals given 12.5 mg marbofloxacin/lb. Macroscopically, these lesions were vesicles, raised areas, or depressed, light-colored areas. Microscopically, these lesions were characterized by the presence of one or more of the following: fissuring, erosion, chondrocyte proliferation, fibrillation, or vertical splitting of the articular cartilage. These cartilage lesions in treated dogs were similar to those in control dogs, and were not typical of those produced by fluoroquinolones. In addition to the above pathologic alterations, red areas of articular cartilage were noted macroscopically in 0/8 placebo-treated dogs and in 2/8 dogs from each of the three marbofloxacin-treated groups. These areas usually correlated microscopically with areas of vascularity of the articular surface, but could not be confirmed microscopically in all animals. They consisted of large blood vessels in mature fibrous connective tissue, with no indication of active vascularization due to drug-induced damage. They were considered most likely to be developmental anomalies or normal variations of the joint surface and were not considered to be related to drug treatment.

    Marbofloxacin was administered to 12- to 14-month-old beagle dogs at a dosage of 25 mg/lb/day for 12 days. Decreased food consumption, vomiting, dehydration, excessive salivation, tremors, reddened skin, facial swelling, decreased activity and weight loss were seen in treated dogs. No clinical lameness was noted. As in the 42 day study, grossly visible, focal, red areas of articular cartilage were seen. These findings were noted in 2/6 placebo-treated dogs and in 4/6 marbofloxacin-treated dogs. The foci were areas of fibrocartilage with prominent vascularization or increased vascularization of subchondral bone. Due to the appearance microscopically and macroscopically, these red foci were described as likely to be developmental anomalies or normal variations in articular cartilage.

    Marbofloxacin administered to 3- to 4-month-old, large breed, purpose-bred mongrel dogs at a dosage of 5 mg/lb/day for 14 days resulted in marked lameness in all dogs due to articular cartilage lesions. Lameness was accompanied by decreased appetite and activity.

    Cats: Marbofloxacin was administered for 42 consecutive days to 24 cats approximately 8 months old (8 cats per treatment group) at the dosages of 2.5, 7.5 and 12.5 mg/lb/day (5.5, 16.5 and 27.5 mg/kg/day). Treatment with marbofloxacin did not produce adverse effects on body weights, food consumption, serum chemistry, urinalysis or organ weight parameters. Decreased segmented neutrophil counts were observed in some cats in all treatment groups, including the placebo group, but mean counts were significantly lower in the marbofloxacin-treated groups. In some cats, absolute neutrophil counts were below normal reference values (as low as 615 neutrophils/μL in a marbofloxacin-treated cat and as low as 882 neutrophils/μL in a placebo-treated cat). Other hematological observations were not adversely affected. Clinical signs were occasionally noted in cats in the highest dosage group: excessive salivation in 4/8 cats and redness of ear pinnae in 2/8 cats. Macroscopic changes in the articular cartilage of femurs were seen in one cat receiving 7.5 mg/lb and in 3 cats receiving 12.5 mg/lb. Microscopically, these gross lesions were related to a focal or multifocal chondropathy.

    Microscopic chondropathy not associated with macroscopic observations was also present in one cat treated with 2.5 mg/lb daily (1× the upper end of the dose range) and one additional cat treated with 7.5 mg/lb daily. There was no evidence of lameness during the course of the study.

    A perivascular to diffuse dermatitis was seen microscopically in one mid-dose cat and 4 high-dose cats. Funduscopic exam by a board-certified ophthalmologist and histologic examination of retina and optic nerve by ocular pathologists revealed no lesions in any of the treatment groups.

    Marbofloxacin was also administered orally to 6 cats approximately 8 months of age for 14 consecutive days at a dosage of 25 mg/lb/day (55 mg/kg/day). Clinical signs associated with drug intolerance were excessive salivation in 5/6 cats and redness of ear pinnae in all cats after 8 days of treatment. Emesis was noted occasionally in several cats and diminished activity was noted in one cat. Decreased food intake was noted in some animals, primarily males, when compared to controls. Perivascular to diffuse dermatitis was seen microscopically in the pinnae of all treated animals and in the standard skin samples of several animals. There was focal or multifocal articular chondropathy in 2/6 treated animals. One treated cat had a duodenal mucosal erosion and one treated cat had a pyloric ulcer. There were no observations of lameness and no adverse effects on hematology, clinical chemistry, urinalysis, or organ weight parameters. Funduscopic examination by a board-certified ophthalmologist and histologic examination of retina and optic nerve by ocular pathologists revealed no lesions.

    A study was conducted to investigate the effect of marbofloxacin on articular cartilage of skeletally mature cats 12-14 months of age. Forty cats were randomly assigned to 4 groups of 10 cats each. Groups received placebo or marbofloxacin at dosages of 1.25, 3.75 or 7.5 mg/lb/day (2.75, 8.25 or 16.5 mg/kg/day) for 42 consecutive days. There were no treatment-related pathological changes in the joints or other tissues. Emesis and soft stools was noted in all treatment groups, including placebo, and increased in frequency with increasing dose and duration of treatment. Emesis was more apparent in the high-dose males.

  • STORAGE AND HANDLING

    STORAGE CONDITIONS: Store at controlled room temperature, 68-77°F (20-25°C).

  • HOW SUPPLIED

    HOW SUPPLIED: Marboquin tablets are available in the following strengths of marbofloxacin and bottle sizes:

    25 mg scored tablets supplied in bottles containing
    100 tabletsNDC 17033-125-10
    250 tabletsNDC 17033-125-25
    50 mg scored tablets supplied in bottles containing
    100 tabletsNDC 17033-126-10
    250 tabletsNDC 17033-126-25
    100 mg scored tablets supplied in a bottle containing
    50 tabletsNDC 17033-127-50
    200 mg scored tablets supplied in a bottle containing
    50 tabletsNDC 17033-128-50
  • REFERENCES:

    1. Schneider M, et al: Pharmacokinetics of marbofloxacin in dogs after oral and parenteral administration. J Vet Pharmacol Therap 19:56-61, 1996.

    To report suspected adverse effects, and/or obtain a copy of the SDS, call (866) 933-2472.

    Approved by FDA under ANADA # 200-586

  • SPL UNCLASSIFIED SECTION

    Manufactured for:
    Dechra Veterinary Products
    7015 College Boulevard, Suite 525
    Overland Park, KS 66211 USA

    Rev. 05/19

  • PRINCIPAL DISPLAY PANEL - 25 mg Tablet Bottle Label

    25 mg

    Marboquin™ (marbofloxacin)
    Tablets
    Antibacterial
    25 mg

    For oral use in dogs and cats only

    Caution: Federal law restricts this drug to use by or on the
    order of a licensed veterinarian.

    Federal law prohibits the extralabel use
    of this drug in food-producing animals.

    100 tablets

    Approved by FDA under ANADA # 200-586

    Dechra

    PRINCIPAL DISPLAY PANEL - 25 mg Tablet Bottle Label
  • PRINCIPAL DISPLAY PANEL - 50 mg Tablet Bottle Label

    50 mg

    Marboquin™ (marbofloxacin)
    Tablets
    Antibacterial
    50 mg

    For oral use in dogs only

    Caution: Federal law restricts this drug to use by or on the
    order of a licensed veterinarian.

    Federal law prohibits the extralabel use
    of this drug in food-producing animals.

    100 tablets

    Approved by FDA under ANADA # 200-586

    Dechra

    PRINCIPAL DISPLAY PANEL - 50 mg Tablet Bottle Label
  • PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label

    100 mg

    Marboquin™ (marbofloxacin)
    Tablets
    Antibacterial
    100 mg

    For oral use in dogs only

    Caution: Federal law restricts this drug to use
    by or on the order of a licensed veterinarian.

    Federal law prohibits the extralabel use
    of this drug in food-producing animals.

    50 tablets

    Approved by FDA under ANADA # 200-586

    Dechra

    PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label
  • PRINCIPAL DISPLAY PANEL - 200 mg Tablet Bottle Label

    200 mg

    Marboquin™ (marbofloxacin)
    Tablets
    Antibacterial
    200 mg

    For oral use in dogs only

    Caution: Federal law restricts this drug to use
    by or on the order of a licensed veterinarian.

    Federal law prohibits the extralabel use
    of this drug in food-producing animals.

    50 tablets

    Approved by FDA under ANADA # 200-586

    Dechra

    PRINCIPAL DISPLAY PANEL - 200 mg Tablet Bottle Label
  • INGREDIENTS AND APPEARANCE
    MARBOQUIN 
    marbofloxacin tablet
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:17033-125
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    marbofloxacin (UNII: 8X09WU898T) (marbofloxacin - UNII:8X09WU898T) marbofloxacin25 mg
    Product Characteristics
    ColorPINKScore2 pieces
    ShapeOVALSize10mm
    FlavorImprint Code 25;MG;D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17033-125-10100 in 1 BOTTLE
    2NDC:17033-125-25250 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20058610/14/2020
    MARBOQUIN 
    marbofloxacin tablet
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:17033-126
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    marbofloxacin (UNII: 8X09WU898T) (marbofloxacin - UNII:8X09WU898T) marbofloxacin50 mg
    Product Characteristics
    ColorPINKScore2 pieces
    ShapeOVALSize13mm
    FlavorImprint Code 50;MG;D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17033-126-10100 in 1 BOTTLE
    2NDC:17033-126-25250 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20058610/14/2020
    MARBOQUIN 
    marbofloxacin tablet
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:17033-127
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    marbofloxacin (UNII: 8X09WU898T) (marbofloxacin - UNII:8X09WU898T) marbofloxacin100 mg
    Product Characteristics
    ColorPINKScore2 pieces
    ShapeOVALSize16mm
    FlavorImprint Code 100;MG;D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17033-127-5050 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20058610/14/2020
    MARBOQUIN 
    marbofloxacin tablet
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:17033-128
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    marbofloxacin (UNII: 8X09WU898T) (marbofloxacin - UNII:8X09WU898T) marbofloxacin200 mg
    Product Characteristics
    ColorPINKScore2 pieces
    ShapeOVALSize19mm
    FlavorImprint Code 200;MG;D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17033-128-5050 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20058610/14/202006/05/2024
    Labeler - Dechra Veterinary Products LLC (362142734)