CLOMIPRAMINE HYDROCHLORIDE tablet
clomipramine hydrochloride by
Drug Labeling and Warnings
clomipramine hydrochloride by is a Animal medication manufactured, distributed, or labeled by Covetrus North America. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Caution:
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Description:
Clomipramine Hydrochloride Tablets belong to the dibenzazepine class of tricyclic antidepressants. Clomipramine hydrochloride is 3-chloro-5[3-(dimethyl-amino)propyl]-10,11 dihydro-5H dibenz[b,f]azepine monohydrochloride. Clomipramine Hydrochloride Tablets are oblong, light brown in color and contain clomipramine hydrochloride formulated together with meat components. The molecular weight of clomipramine hydrochloride is 351.3. The structural formula is:
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Clinical Pharmacology:
Clomipramine hydrochloride reduces the clinical signs of separation anxiety by affecting serotonergic and noradrenergic neuronal transmission in the central nervous system. While clomipramine hydrochloride can cause lethargy in dogs (see Adverse Reactions) its mode of action is not as a sedative. Clomipramine hydrochloride’s capacity to inhibit re-uptake of serotonin in the central nervous system is believed to be the primary mechanism of action. Clomipramine hydrochloride is rapidly absorbed when administered orally. A single-dose crossover study involving 12 dogs evaluated clomipramine hydrochloride bioavailability after IV (2 mg/kg) and oral (4 mg/kg) administration in either a fed or fasted state. The administration of clomipramine hydrochloride in the presence of food resulted in an increase in the rate and extent of drug absorption as shown in the following table (mean ±SD):
AUC0-inf
(nmol hr/L)Cmax
(nmol/L)Tmax
(hr)Absolute
Bioavailability
(F)Fed 1670 ± 575 601 ± 286 1.18 ± 0.32 0.21 ± 0.07 Fasted 1350 ± 447 379 ± 154 1.31 ± 0.32 0.17 ± 0.05 The absolute bioavailability is approximately 25% greater in fed dogs. The apparent terminal plasma half-life ranges from approximately 2 to 9 hours in fed and 3 to 21 hours in fasted dogs. The difference and variability in apparent half-life estimates may be attributable to prolonged drug absorption in the fasted state. The relatively large volume of distribution (3.8 ±0.8 L/kg) suggests that the drug is widely distributed throughout the body. Clomipramine is primarily metabolized in the liver.
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Indications & Usage:
Clomipramine Hydrochloride Tablets are to be used as part of a comprehensive behavioral management program to treat separation anxiety in dogs greater than 6 months of age. Inappropriate barking or destructive behavior, as well as inappropriate elimination (urination or defecation) may be alleviated by the use of Clomipramine Hydrochloride Tablets in conjunction with behavior modification.
Separation anxiety is a complex behavior disorder displayed when the owner (or other attachment figure) leaves the dog. The signs of separation anxiety evaluated in controlled trials were vocalization, destructive behavior, excessive salivation, and inappropriate elimination. In the absence of the owner or attachment figure, dogs with separation anxiety may exhibit one or more of these clinical signs. Although the owner (attachment figure) may inadvertently misinterpret this behavior, which only happens in their absence, as spiteful, it is thought to be the result of anxiety experienced by the dog. Punishment is not considered appropriate for a dog with separation anxiety.
Proper recognition of clinical signs, including a complete patient history and assessment of the patient’s household environment, is essential to accurately diagnose and treat separation anxiety.
The use of Clomipramine Hydrochloride Tablets should not replace appropriate behavioral and environmental management but should be used to facilitate a comprehensive behavior management program.
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Contraindications:
Clomipramine Hydrochloride Tablets are contraindicated in dogs with known hypersensitivity to clomipramine or other tricyclic antidepressants.
Clomipramine Hydrochloride Tablets should not be used in male breeding dogs. Testicular hypoplasia was seen in dogs treated for 1 year at 12.5 times the maximum daily dose.
Clomipramine Hydrochloride Tablets should not be given in combination, or within 14 days before or after treatment with a monoamine oxidase inhibitor [e.g. selegiline hydrochloride (L-deprenyl),amitraz].
Clomipramine Hydrochloride Tablets are contraindicated for use in dogs with a history of seizures or concomitantly with drugs which lower the seizure threshold.
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Human Warnings:
Not for use in humans. Keep out of reach of children. In case of accidental ingestion seek medical attention immediately. In children, accidental ingestion should be regarded as serious. There is no specific antidote for clomipramine. Overdose in humans causes anticholinergic effects including effects on the central nervous (e.g., convulsions) and cardiovascular (e.g., arrhythmia, tachycardia) systems. People with known hypersensitivity to clomipramine should administer the product with caution.
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Precautions:
General: Clomipramine Hydrochloride Tablets are not recommended for other behavior problems, such as aggression (see Adverse Reactions). Studies to establish the safety and efficacy of clomipramine hydrochloride tablets in dogs less than 6 months of age have not been conducted.
Diagnosis: It is critical to conduct a comprehensive physical examination, including appropriate laboratory tests, and to obtain a thorough history and assessment of the patient’s household environment, to rule-out causes of inappropriate behavior unrelated to separation anxiety before prescribing Clomipramine Hydrochloride Tablets. Periodic reassessment of hematological and serum biochemical data during the administration of this medication is advised. Veterinarians should be familiar with the risks and benefits of the treatment of behavioral disorders in dogs before initiating therapy. Inappropriate use of Clomipramine Hydrochloride Tablets, i.e., in the absence of a diagnosis or without concurrent behavioral modification, may expose the animal to unnecessary adverse effects and may not provide any lasting benefit of therapy.
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Drug Interactions:
Recommendations on the interaction between clomipramine and other medications are extrapolated from data generated in humans. Plasma levels of tricyclic antidepressants have been reported to be decreased by the concomitant administration of hepatic enzyme inducers (e.g., barbiturates, phenytoin); therefore plasma concentrations of clomipramine may be decreased by the concomitant administration of phenobarbital. Plasma levels of closely related tricyclic antidepressants have been reported to be increased by the concomitant administration of hepatic enzyme inhibitors (e.g., cimetidine, fluoxetine). Tricyclic antidepressants themselves may exhibit hepatic enzyme inhibition and possibly increase plasma levels of barbiturates (phenobarbital). Caution is advised in using clomipramine with anticholinergic or sympathomimetic drugs or with other CNS-active drugs, including general anesthetics and neuroleptics.
Prior to elective surgery with general anesthetics, clomipramine should be discontinued for as long as clinically feasible.
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Use in Concomitant Illness:
Use with caution in dogs with cardiovascular disease. At 20 mg/kg/day (5X the maximum recommended dose), bradycardia and arrhythmias (atrioventricular node block and ventricular extrasystole) were observed in dogs. Because of its anticholinergic properties, clomipramine should be used with caution in patients with increased intraocular pressure, a history of narrow angle glaucoma, urinary retention or reduced gastrointestinal motility. Because clomipramine is principally metabolized in the liver, caution is advised in using this medication in the presence of preexisting liver disease.
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Reproductive Safety:
Safety studies to determine the effects of clomipramine hydrochloride tablets in pregnant or lactating female dogs have not been conducted. Clomipramine Hydrochloride Tablets should not be used in breeding males (see Contraindications).
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Efficacy:
Dose Establishment: A 12 week, placebo-controlled, multi-site clinical trial was conducted in the US and Europe to establish an effective dose of clomipramine hydrochloride tablets in dogs. Treatment with clomipramine hydrochloride tablets, at 2 - 4 mg/kg/day divided twice daily, in conjunction with behavioral modification (desensitization and counterconditioning) was more effective than behavior modification alone in reducing the signs of separation anxiety in dogs.
Dose Confirmation: In another placebo-controlled, multi-site clinical trial, clomipramine hydrochloride tablets at 2 - 4 mg/kg/day given either once daily or divided twice daily showed significant improvement in resolving signs of separation anxiety when tested against behavioral modification alone (desensitization and counterconditioning). In this 8 week study, the rate of improvement of the dogs receiving clomipramine hydrochloride tablets with behavioral modification was significantly faster than the rate of improvement of the dogs receiving behavioral modification alone. After one week on trial, 47% of the dogs receiving clomipramine hydrochloride tablets once or twice (divided dose) daily in conjunction with behavioral modification showed clinical improvement compared to improvement in 29% of the dogs receiving behavioral modification alone.
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Safety:
Clomipramine hydrochloride tablets were demonstrated to be well-tolerated in dogs at the recommended label dose of 2-4 mg/kg/day. In a six month target animal safety study, beagle dogs were dosed daily at 4 (1X), 12 (3X), and 20 (5X) mg/kg/day. Emesis was seen in all groups including the dogs receiving placebo, but occurred more frequently in dogs receiving 12 and 20 mg/kg. Decreased activity was also seen in dogs receiving the 12 and 20 mg/kg. There were no apparent treatment-related alterations in the following: body weights, physical examination findings, electrocardiograph examinations, hematology or biochemistry parameters, ophthalmoscopic examinations, macroscopic or microscopic organ examinations and organ weights. Average food and water consumption over the 26 week period was similar for control and treated groups. In a one year study, pure bred dogs were dosed daily at 12.5 (3X), 50 (12.5X), and 100 (25X) mg/kg/day. Emesis and mydriasis were observed within 15 minutes to one hour after dosing in dogs receiving 12.5, 50, and 100 mg/kg/day and lethargy was observed within 1 hour of dosing in dogs receiving 50 and 100 mg/kg. Testicular hypoplasia was seen in dogs receiving 50 mg/kg. At 100 mg/kg/day (25X) convulsions and eventual death occurred in five out of the eight dogs.
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Adverse Reactions:
Frequency and category of adverse reactions observed in dogs dosed with clomipramine hydrochloride tablets or placebo were observed in multisite clinical studies as follows.
Adverse Reactions Reported in
Placebo-Controlled Clinical Field TrialsClomipramine Hydrochloride Tablets
N=180Placebo
N=88Emesis 36 (20%) 8 (9%) Lethargy 26 (14%) 7 (8%) Diarrhea 17 (9%) 4 (5%) Polydipsia 6 (3%) 0 Decreased Appetite 6 (3%) 3 (3%) Aggression* 3 (2%) 1 (1%) Seizure 2 (1%) 0 Dry Mouth 1 (0.5%) 1 (1%) Tremors 1 (0.5%) 0 Constipation 1 (0.5%) 0 Anisoconia 1 (0.5%) 0 Polyuria 1 (0.5%) 0 Hyperthermia 1 (0.5%) 0 *These dogs displayed growling behavior towards either humans or other dogs.
Post-Approval Experience: Although not all adverse reactions are reported, the following adverse reactions are based on voluntary post-approval adverse drug experience reporting: lethargy/depression, anorexia, elevation in liver enzymes, vomiting and diarrhea. Hepatobiliary disease has occurred, especially in the presence of pre-existing conditions or with concurrent administration of drugs metabolized via the hepatic system. Additionally, in an overdose situation, the following signs have been reported: ataxia, convulsion(s), anticholinergic effects (e.g. mydriasis, bradycardia, tachycardia, and arrhythmia) and vocalization.
The Safety Data Sheet (SDS) contains more detailed occupational safety information.
To report suspected adverse reactions, call (855) 724-3461. In case of accidental human ingestion, call 1-561-570-1875.
For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or http://www.fda.gov/AnimalVeterinary/SafetyHealth.
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Dosage & Administration:
The recommended daily dose of Clomipramine Hydrochloride Tablets is 2 to 4 mg/kg/day (0.9 -1.8 mg/lb/day) (see dosing table below). It can be administered as a single daily dose or divided twice daily based on patient response and/or tolerance of the side effects. It may be prudent to initiate treatment in divided doses to minimize side effects by permitting tolerance to side effects to develop or allowing the patient time to adapt if tolerance does not develop. To reduce the incidence of vomiting that may be experienced by some dogs, Clomipramine Hydrochloride Tablets may be given with a small amount of food.
Dog Weight
(lbs)Clomipramine Hydrochloride Tablets
per DayNo. Tablets
per DayTablet
Strength2.75 - 5.5 5 mg 1 5 mg 5.6 - 10.9 10 mg 2 5 mg 11 - 22 20 mg 1 20 mg 22.1 - 44 40 mg 1 40 mg 44.1 - 88 80 mg 1 80 mg 88.1 - 176 160 mg 2 80 mg The specific methods of behavioral modification used in clinical trials involved desensitization and counterconditioning techniques. Since the manifestation of separation anxiety can vary according to the individual dog, it is advised that a specific behavior modification plan be developed based on a professional assessment of each individual case.
Once the desired clinical effect is achieved and the owners have successfully instituted the appropriate behavioral modification, the dose of Clomipramine Hydrochloride Tablets may be reduced to maintain the desired effect or discontinued. Withdrawal side effects were not reported in studies with clomipramine hydrochloride tablets in dogs. However, in clinical practice, it is recommended to taper the individual patient dose while continuing to monitor the dog’s behavior and clinical status through the dose reduction or withdrawal period. Continued behavioral modification is recommended to prevent recurrence of the clinical signs.
The effectiveness and clinical safety of clomipramine hydrochloride tablets for long-term use (i.e., for more than 12 weeks) has not been evaluated.
Professional judgment should be used in monitoring the patient’s clinical status, response to therapy and tolerance to side effects to determine the need to continue treatment with Clomipramine Hydrochloride Tablets and to continue to rule-out physiological disorders which may complicate the diagnosis and treatment of separation anxiety.
- Storage Conditions:
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How Supplied:
Clomipramine Hydrochloride Tablets are available in 5, 20, 40, and 80 mg tablet strengths in color-coded packaging for oral administration to dogs.
Keep this and all drugs out of reach of children.
Distributed by: Covetrus North America
400 Metro Place North, Dublin, OH 43017 covetrus.comApproved by FDA under ANADA # 200-635
REV: 0320 AH-clomipramine-01 - Caution:
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Introduction:
Mizner Bioscience, LLC encourages you to take the time to read this package insert which describes the use of Clomipramine Hydrochloride Tablets for the treatment of separation anxiety in conjunction with behavior modification (training) in dogs. Clomipramine Hydrochloride Tablets do not act as a sedative. Instead, Clomipramine Hydrochloride Tablets help to reduce the anxiety associated with this condition, thus allowing your dog to more effectively benefit from behavior training. After reading this insert, if you have any questions about the use of Clomipramine Hydrochloride Tablets, please consult your veterinarian.
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Description:
Clomipramine Hydrochloride Tablets belong to the dibenzazepine class of tricyclic antidepressants. Clomipramine hydrochloride is 3-chloro-5[3-(dimethyl-amino)propyl]-10,11 dihydro-5H dibenz[b,f] azepine monohydrochloride. Clomipramine Hydrochloride Tablets are oblong, light brown in color and contain clomipramine hydrochloride formulated together with meat components.
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Indications and Usage:
Clomipramine Hydrochloride Tablets are to be used as part of a comprehensive behavioral management program to treat separation anxiety in dogs greater than 6 months of age. Inappropriate barking or destructive behavior, as well as inappropriate elimination of (urination or defecation) may be alleviated by the use of Clomipramine Hydrochloride Tablets in conjunction with behavior modification.
Separation anxiety is a complex behavior disorder displayed when the owner (or other attachment figure) leaves the dog. In the absence of the owner or attachment figure, dogs with separation anxiety may exhibit one or more clinical signs. The signs of separation anxiety evaluated in controlled trials were vocalization, destructive behavior, excessive salivation, and inappropriate elimination. Although it may appear that this behavior, which only happens in the dog owner’s absence, is a spiteful action, this behavior is thought to be a result of anxiety experienced by the dog. Therefore, punishment would not be appropriate for the dog with this behavior.
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Behavior Modification (Training):
Behavior training is a necessary component of therapy with Clomipramine Hydrochloride Tablets. In clinical trials, specific behavior training techniques were used at the following times:
- when the owner interacted with the dog while at home
- when the owner was preparing to leave the home
- when the owner returned home and greeted the dog
Since the methods used for behavior training can vary according to patient needs, it is important that you follow the instructions provided by your veterinarian regarding the specific techniques recommended for modifying your dog’s behavior.
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Contraindications:
Clomipramine Hydrochloride Tablets are contraindicated in dogs with known hypersensitivity to clomipramine or related tricyclic antidepressants.
Clomipramine Hydrochloride Tablets should not be used in male breeding dogs. Testicular hypoplasia was seen in dogs treated for 1 year at 12.5 times the maximum daily dose.
Clomipramine Hydrochloride Tablets should not be given in combination, or within 14 days before or after treatment with a monoamine oxidase inhibitor [e.g. selegiline hydrochloride (L-deprenyl), amitraz].
Clomipramine Hydrochloride Tablets are contraindicated for use in dogs with a history of seizures or concomitantly with drugs which lower the seizure threshold.
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Human Warnings:
Not for use in humans. KEEP OUT OF REACH OF CHILDREN.
In case of accidental ingestion seek medical attention immediately. In children, accidental ingestion should be regarded as serious. There is no specific antidote for clomipramine.
Overdose in humans causes anticholinergic effects including effects on the central nervous (e.g., convulsions) and cardiovascular (e.g., arrhythmia, tachycardia) systems. People with known hypersensitivity to clomipramine should administer the product with caution. -
Precautions:
It is important that your dog be closely monitored by your veterinarian while on a treatment plan with Clomipramine Hydrochloride Tablets and behavior training. You must inform your veterinarian of any current or future medications you are administering to your dog. The use of Clomipramine Hydrochloride Tablets in conjunction with certain other drugs or when your dog has other illnesses may be contraindicated or increase the risks of adverse reactions.
It is important that you inform your veterinarian of any changes in your dog’s environment including, but not limited to, a new family member, a new pet, a move to a new location, or a change in your existing daily schedule. Some changes may result in an altered
response to therapy.It is important to inform your veterinarian of any perceived changes in your dog’s behavior, appetite, or overall health while administering any medication. Some dogs display a temporary lethargy with the first few days of clomipramine hydrochloride tablets treatment. In some cases, signs of separation anxiety, such as vocalization, may temporarily increase at the initiation of treatment. In an overdose situation, seek veterinary attention for your pet as soon as possible.
The safety and efficacy of clomipramine hydrochloride tablets have not been established in dogs less than 6 months of age or in pregnant or lactating female dogs. Clomipramine Hydrochloride Tablets should not be used in breeding male dogs (see Contraindications). Clomipramine Hydrochloride Tablets are not recommended for other behavior problems, such as aggression.
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Efficacy:
Clomipramine hydrochloride tablets were tested in clinical trials involving client-owned dogs to determine effectiveness.
Clomipramine hydrochloride tablets, at 2 – 4 mg/kg/day (0.9 – 1.8 mg/pound/day) when used in conjunction with behavior training accelerated both the time to improvement and the final result of separation anxiety therapy compared to behavioral training alone.
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Adverse Reactions:
The following adverse reactions have been reported associated with administration of clomipramine hydrochloride tablets:
lethargy/depression, vomiting, diarrhea, elevation in liver enzymes, convulsion(s), increased heart rate, decreased heart rate, increased thirst and confusion. Liver disease has occurred, especially in the presence of pre-existing conditions or with concurrent administration of drugs metabolized by the liver.
In overdoses, signs such as vomiting, lethargy or depression, weakness and incoordination, dilated pupils, and vocalization may occur. Consult with your veterinarian if your dog experiences these or any other conditions.In case of accidental human ingestion or accidental overdose in dogs, call 1-561-570-1875.
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Dosage and Administration:
The recommended daily dose of Clomipramine Hydrochloride Tablets is 2 to 4 mg/kg/day (0.9 – 1.8 mg/lb/day) (see dosing table below).
Your veterinarian will instruct you to give the drug either once a day or divide the daily dose into 2 separate doses depending on your dog’s response to the drug or tolerance to any side effects.
Clomipramine Hydrochloride Tablets may be given with a small amount of food in an attempt to reduce the incidence of vomiting that may be experienced by some dogs. If a dose is missed, the next dose should be administered (without doubling) at the next scheduled dosing time.Dog Weight
(lbs)Clomipramine Hydrochloride Tablets
per DayNo. Tablets
per DayTablet
Strength2.75 - 5.5 5 mg 1 5 mg 5.6 - 10.9 10 mg 2 5 mg 11 - 22 20 mg 1 20 mg 22.1 - 44 40 mg 1 40 mg 44.1 - 88 80 mg 1 80 mg 88.1 - 176 160 mg 2 80 mg Your veterinarian may decrease the dose or discontinue treatment with Clomipramine Hydrochloride Tablets depending on your dog’s response to treatment. Continued behavior training is recommended, even after cessation of drug therapy.
- Storage Conditions:
- How Supplied:
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLOMIPRAMINE HYDROCHLORIDE
clomipramine hydrochloride tabletProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC: 11695-6950 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOMIPRAMINE HYDROCHLORIDE (UNII: 2LXW0L6GWJ) (CLOMIPRAMINE - UNII:NUV44L116D) CLOMIPRAMINE HYDROCHLORIDE 5 mg Product Characteristics Color BROWN (light brown speckled) Score 2 pieces Shape OVAL (modified capsule shaped) Size 9mm Flavor MEAT (beef) Imprint Code MB;113 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 11695-6950-3 30 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200635 12/15/2019 CLOMIPRAMINE HYDROCHLORIDE
clomipramine hydrochloride tabletProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC: 11695-6951 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOMIPRAMINE HYDROCHLORIDE (UNII: 2LXW0L6GWJ) (CLOMIPRAMINE - UNII:NUV44L116D) CLOMIPRAMINE HYDROCHLORIDE 20 mg Product Characteristics Color BROWN (light brown speckled) Score 2 pieces Shape OVAL (modified capsule shaped) Size 11mm Flavor MEAT (beef) Imprint Code MB;114 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 11695-6951-3 30 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200635 12/15/2019 CLOMIPRAMINE HYDROCHLORIDE
clomipramine hydrochloride tabletProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC: 11695-6952 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOMIPRAMINE HYDROCHLORIDE (UNII: 2LXW0L6GWJ) (CLOMIPRAMINE - UNII:NUV44L116D) CLOMIPRAMINE HYDROCHLORIDE 40 mg Product Characteristics Color BROWN (light brown speckled) Score 2 pieces Shape OVAL (modified capsule shaped) Size 15mm Flavor MEAT (beef) Imprint Code MB;115 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 11695-6952-3 30 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200635 12/15/2019 CLOMIPRAMINE HYDROCHLORIDE
clomipramine hydrochloride tabletProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC: 11695-6953 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOMIPRAMINE HYDROCHLORIDE (UNII: 2LXW0L6GWJ) (CLOMIPRAMINE - UNII:NUV44L116D) CLOMIPRAMINE HYDROCHLORIDE 80 mg Product Characteristics Color BROWN (light brown speckled) Score 2 pieces Shape OVAL (modified capsule shaped) Size 15mm Flavor MEAT (beef) Imprint Code MB;116 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 11695-6953-3 30 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200635 12/15/2019 Labeler - Covetrus North America (603750329)
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