Animal NDC 11695-4024-1 Xylazine

Animal Product Information

Field Name Field Value
Animal NDC Code 11695-4024-1
Proprietary Name Xylazine What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Xylazine What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Labeler Name Covetrus
Product Type Prescription Animal Drug
Usage Information
    INDICATIONSXylazine (xylazine injection) should be used in horses and Cervidae (Fallow Deer, Mule Deer, Sika Deer, White-Tailed Deer, and Elk) when it is desirable to produce a state of sedation accompanied by a shorter period of analgesia.Horses: Xylazine (xylazine injection) has been used successfully as follows:1. Diagnostic procedures-oral and ophthalmic examinations, abdominal palpation, rectal palpation, vaginal examination, catheterization of    the bladder and radiographic examinations.2. Orthopedic procedures, such as application of casting materials and splints.3. Dental procedures.4. Minor surgical procedures of short duration such as debridement, removal of cutaneous neoplasms and suturing of lacerations.5. To calm and facilitate handling of fractious animals.6. Therapeutic medication for sedation and relief of pain following injury or surgery.7. Major surgical procedures:   a. When used as a preanesthetic to general anesthesia.   b. When used in conjunction with local anesthetics.Cervidae: Xylazine (xylazine injection) may be used for the following:1. To calm and facilitate handling of fractious animals.2. Diagnostic procedures.3. Minor surgical procedures.4. Therapeutic medication for sedation and relief of pain following injury or surgery.5. As a preanesthetic to local anesthesia.Xylazine at the recommended dosages can be used in conjunction with local anesthetics, such as procaine or lidocaine.
Active Ingredient(s)
  • Xylazine Hydrochloride
Inactive Ingredient(s)
  • METHYLPARABEN (A2I8C7HI9T)
  • PROPYLPARABEN (Z8IX2SC1OH)
  • METHYLPARABEN (A2I8C7HI9T)
  • PROPYLPARABEN (Z8IX2SC1OH)
Marketing Category ANADA - ABBREVIATED NEW ANIMAL DRUG APPLICATION What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number ANADA200529 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Xylazine Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Description



Xylazine
(xylazine injection)
100 mg/mL
Sedative and Analgesic For Use In Horses and Cervidae Only

DESCRIPTION
Xylazine (xylazine injection) is supplied in 50 mL multipledose vials as a sterile solution. Each mL contains 100 mg xylazine (xylazine base equivalent); 0.9 mg methylparaben; 0.1 mg propylparaben; water for injection; citric acid and sodium citrate for pH adjustment to 5.5 ± 0.3.

ACTIVE INGREDIENT:
Xylazine hydrochloride ..................................................................................... 11.7% (Equivalent to 10% base)
INERT INGREDIENTS:......................................................................................88.3%
                                                                                                                        100.0%

CAUTION
Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not use in Cervidae less than 15 days before or during the hunting season.


Animal Pharmacology & Or Toxicology



PHARMACOLOGY
Xylazine, a non-narcotic compound, is a sedative and analgesic as well as muscle relaxant. Its sedative and analgesic activity is related to central nervous system depression. Its muscle- relaxant effect is based on inhibition of the intraneural transmission of impulses in the central nervous system. The principal pharmacological activities develop within 10 to 15 minutes after intramuscular injection, and within 3 to 5 minutes following intravenous administration in horses.

A sleeplike state, the depth of which is dose-dependent, is usually maintained for 1 to 2 hours, while analgesia lasts from 15 to 30 minutes. The centrally-acting muscle relaxant effect causes relaxation of the skeletal musculature, complementing sedation and analgesia.

In horses and Cervidae under the influence of Xylazine (xylazine injection), the respiratory rate is reduced as in natural sleep. Following treatment with Xylazine (xylazine injection), the heart rate is decreased and a transient change in the conductivity of the cardiac muscle may occur, as evidenced by a partial atrioventricular block. This resembles the atrioventricular block often observed in normal horses.1,2,3,4 Although a partial A-V block may occasionally occur following intramuscular injection of Xylazine (xylazine injection), the incidence is less than when it is administered intravenously. Intravenous administration of Xylazine (xylazine injection) causes a transient rise in blood pressure, followed by a slight decrease.

Xylazine has no effect on blood clotting time or other hematologic parameters.


Indications & Usage



INDICATIONS
Xylazine (xylazine injection) should be used in horses and Cervidae (Fallow Deer, Mule Deer, Sika Deer, White-Tailed Deer, and Elk) when it is desirable to produce a state of sedation accompanied by a shorter period of analgesia.

Horses: Xylazine (xylazine injection) has been used successfully as follows:
1. Diagnostic procedures-oral and ophthalmic examinations, abdominal palpation, rectal palpation, vaginal examination, catheterization of    the bladder and radiographic examinations.
2. Orthopedic procedures, such as application of casting materials and splints.
3. Dental procedures.
4. Minor surgical procedures of short duration such as debridement, removal of cutaneous neoplasms and suturing of lacerations.
5. To calm and facilitate handling of fractious animals.
6. Therapeutic medication for sedation and relief of pain following injury or surgery.
7. Major surgical procedures:
   a. When used as a preanesthetic to general anesthesia.
   b. When used in conjunction with local anesthetics.

Cervidae: Xylazine (xylazine injection) may be used for the following:
1. To calm and facilitate handling of fractious animals.
2. Diagnostic procedures.
3. Minor surgical procedures.
4. Therapeutic medication for sedation and relief of pain following injury or surgery.
5. As a preanesthetic to local anesthesia.

Xylazine at the recommended dosages can be used in conjunction with local anesthetics, such as procaine or lidocaine.


Dosage & Administration



DOSAGE AND ADMINISTRATION
1. Horse Dosage:

   Intravenously−0.5 mL/100 lbs body weight (0.5 mg/lb)
   Intramuscularly−1.0 mL/100 lbs body weight (1.0 mg/lb)

   Following injection of Xylazine (xylazine injection), the animal should be allowed to rest quietly until the full effect has been reached.
   These dosages produce sedation which is usually maintained for 1 to 2 hours, and analgesia which lasts for 15 to 30 minutes.

2. Preanesthetic to Local Anesthesia: Xylazine at the recommended dosages can be used in conjunction with local anesthetics, such as procaine or lidocaine.

3. Preanesthetic to General Anesthesia:Xylazine at the recommended dosage rates produces an additive effect to central nervous system depressants such as pentobarbital sodium, thiopental sodium and thiamylal sodium. Therefore, the dosage of such compounds should be reduced and administered to the desired effect. In general, only 1/3 to 1/2 of the calculated dosage of the barbiturates will be needed to produce a surgical plane of anesthesia.

   Post-anesthetic or emergence excitement has not been observed in animals preanesthetized with Xylazine.

   Xylazine has been used successfully as a preanesthetic agent for pentobarbital sodium, thiopental sodium, thiamylal sodium, nitrous    oxide, ether, halothane, glyceryl guaiacolate, and methoxyflurane anesthesia.

4. Cervidae Dosage: Administer intramuscularly, by either hand syringe or syringe dart, in the heavy muscles of the croup or shoulder.
   Cervidae Dosage Range:
   Fallow Deer (Dama dama)−2.0 to 4.0 mL/100 lbs body weight (2.0 to 4.0 mg/lb).
   Mule Deer (Odocoileus hemionus)−1.0 to 2.0 mL/100 lbs body weight (1.0 to 2.0 mg/lb).
   Sika Deer (Cervus nippon)−1.0 to 2.0 mL/100 lbs body weight (1.0 to 2.0 mg/lb).
   White-Tailed Deer (Odocoileus virginianus)−1.0 to 2.0 mL/100 lbs body weight (1.0 to 2.0 mg/lb).
   Elk (Cervus canadensis)−0.25 to 0.5 mL/100 lbs body weight (0.25 to 0.5 mg/lb).

   Following injection of Xylazine the animal should be allowed to rest quietly until the full effect has been reached.

   These dosages produce sedation which is usually maintained for 1 to 2 hours and analgesia which lasts for 15 to 30 minutes.


Adverse Reactions



SIDE EFFECTS
Xylazine (xylazine injection) in horses and Cervidae, used at recommended dosage levels may occasionally cause slight muscle tremors, bradycardia with partial A-V heart block and a reduced respiratory rate. Movement in response to sharp auditory stimuli may be observed In horses, sweating, rarely profuse, has been reported following administration. In Cervidae, salivation, various vocalizations (bellowing, bleating, groaning, grunting, snoring) on expiration, audible grinding of molar teeth, protruding tongue and elevated temperatures have also been noted in some cases.


Precautions



PRECAUTIONS
Careful consideration should be given before administering to horses or Cervidae with significantly depressed respiration, severe pathologic heart disease, advanced liver or kidney disease, severe endotoxic or traumatic shock, or stress conditions such as extreme heat, cold, high altitude or fatigue.
Do not use Xylazine in conjunction with tranquilizers.
Analgesic effect is variable, and depth should be carefully assayed prior to surgical/clinical procedures. Variability of analgesia occurs most frequently at the distal extremities of horses and Cervidae.

Horses:
Since an additive effect results from the use of Xylazine and the barbiturate compounds, it should be used with caution with these central nervous system depressants. Products known to produce respiratory depression or apnea, such as thiamylal sodium, should be given at a reduced dosage and, when injected intravenously, should be administered slowly. When intravenous administration is desired, avoid perivascular injection in order to achieve the desired effect. Studies have shown negligible evidence of tissue irritation, however, following perivascular injection of xylazine.

Intracarotid Arterial Injection Should Be Avoided. As with many compounds, including tranquilizers, immediate violent seizures followed by collapse may result from inadvertent administration into the carotid artery. Although the reaction with Xylazine (xylazine injection) is usually transient and recovery may be rapid and complete, special care should be taken to assure that the needle is in the jugular vein rather than the carotid artery.

Bradycardia and arrhythmia in the form of incomplete atrioventricular block have been reported following xylazine injection administration. Although clinically the importance of this effect is questioned,1,2,3,4 a standard dose of atropine given prior to or following xylazine injection will greatly decrease the incidence.
Sedation for transport is most successful if actual transportation is begun after the full effect of the drug has been reached and the animal’s stability is maintained while standing. In addition, it should be noted that animals under the influence of Xylazine (xylazine injection) can be aroused by noise or other stimuli and this may increase the risk of injury.

Cervidae:
As in all ruminants, it is preferable to administer Xylazine (xylazine injection) to fasted Cervidae as a safeguard against aspiration of food material into the lungs and/or bloat during deep sedation.

Care should be taken to administer Xylazine (xylazine injection) in the heavy muscles of the croup or shoulder. Injections given subcutaneously, intraperitoneally or into fat deposits will give unpredictable results.

Intra-arterial injection should be avoided. As with many compounds, including tranquilizers, immediate violent seizures followed by collapse may result from inadvertent administration into an artery.

The animal should not be disturbed during induction or until the full effect of the drug has been reached, which is usually 10 to 15 minutes following injection.

The usual time to initial effect of the drug is 2 to 5 minutes. The administrator of the drug should be fully cognizant of this interval prior to administration of drug to free ranging deer or elk, especially at night or in heavily wooded areas.

If the animal has been underdosed (faulty injection or miscalculation on weight) it is advisable to wait one hour before administering a second dose.

Adequate ventilation, especially in cages or crates, is mandatory; keep head and neck in position to insure patent air passage and to prevent aspiration of stomach contents.

During sedation, animals should be prevented from assuming lateral recumbency. A sternal recumbent position is desirable.

While under the effects of Xylazine (xylazine injection) the animal should be protected from an extremely hot or cold environment. Efforts should be made to prevent patient from rising until almost complete recovery is attained.

The transportation of Cervidae given Xylazine (xylazine injection) should be carefully monitored to prevent excessive struggling, injury or death.

Hyperthermic reactions may occur, especially if the subject is in a highly excited state when the drug is administered. Hosing the head and entire body with cold water has usually proven to be an effective deterrent.

The safety of Xylazine (xylazine injection) has not been demonstrated in pregnant Cervidae. Avoid use during the breeding season.

Cervidae should be observed closely until all of the sedative effects of Xylazine (xylazine injection)are gone.

Care should be taken at all times when administering Xylazine (xylazine injection) to Cervidae. This is due to the method of administration (usually darting), the difficulty in estimating body weights and the accepted theory that wild animals are more unpredictable in their response to sedatives and analgesics than the domesticated species.


Warnings And Precautions



WARNINGS
Human Safety: Not for human use. Keep out of reach of children.
   • Strictly avoid self-injection, oral intake and any contact with skin, eyes or mucosa.
   • In the case of accidental contact wash exposed skin or eyes abundantly with water. If symptoms occur, seek medical advice.
   • In the case of accidental oral intake or self-injection, seek the advice of a physician and show the package insert but DO NOT DRIVE.
   • If pregnant women handle the product, special caution should be observed not to self-inject as uterine contractions and decreased fetal       blood pressure may occur after accidental systemic exposure.
   • Users with cardiovascular disease (for example, hypertension or ischemic heart disease) should take special precautions to avoid any       exposure to this product.
   • Caution should be exercised when handling sedated animals. Handling or any other sudden stimuli, including noise, may cause a       defense reaction in an animal that appears to be heavily sedated.

   Note to physician: Xylazine is an alpha2-adrenergic agonist with sedative, some analgesic and muscle relaxant properties. Symptoms    after absorption may include dose-dependent respiratory depression, bradycardia, hypotension, a dry mouth, and hyperglycemia.    Ventricular arrhythmias have also been reported.

   The Safety Data Sheet (SDS) contains more detailed occupational safety information. To report adverse reactions in users or to obtain a    copy of the SDS for this product, contact Bimeda, Inc. at 1-888-524-6332.

Animal safety: This drug should not be administered to domestic food-producing animals. Not for use in horses intended for human consumption.

In Cervidae, occasional capture-associated deaths occur. Clinical trials reveal a mortality rate of approximately 3.5% attendant with the administration of xylazine.


How Supplied



HOW SUPPLIED
Xylazine (xylazine injection) 100 mg/mL for intravenous or intramuscular use is available in 50 mL multiple dose vials.


Storage And Handling



STORAGE
Do not freeze. Store at 20°C- 25°C (68°F to 77°F).


References



REFERENCES

  • Detweiler, D.K.: “The Diagnosis and Significance of Cardiac Arrhythmias.” Progress in Equine Practice. Edited by E.J. Catcott and J.F. Smithcors. American Veterinary Publications, Inc., Santa Barbara, California and Wheaton, Illinois, (1966), 280-281.
  • Glazier, D.B.: “Atrioventricular Heart Block.” Irish Vet. J., Vol. 12, (1958): 194-198.
  • Holmes, J.R., Alps, B.J.: “Observations on Partial Atrioventricular Heart Block in the Horse.” Can. Vet. J., Vol. 7, No. 12, (1966), 280-290.
  • Smetzer, D.L., Smith, C.R., Senta, T.: “Second Degree Atrioventricular Block in the Horse.” Am. J. Vet. Res., Vol. 30, No. 6, (1969), 933-946.
  • To report suspected adverse drug events or for technical assistance, contact Covetrus® at (855) 724-3461. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at www.fda.gov/reportanimalae

    Approved by FDA under ANADA # 200-529

    Questions? (855) 724-3461

    Distributed by:
    Covetrus® North America
    400 Metro Place North
    Dublin, OH 43017
    covetrus.com


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