TULISSIN SOLUTION

Country: Canada

Language: English

Source: Health Canada

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Active ingredient:

TULATHROMYCIN

Available from:

VIRBAC AH, INC.

Dosage:

100MG

Pharmaceutical form:

SOLUTION

Composition:

TULATHROMYCIN 100MG

Administration route:

INTRAMUSCULAR

Units in package:

15G/50G

Prescription type:

Prescription

Therapeutic group:

CATTLE; SWINE (PIGS); SHEEP

Product summary:

Active ingredient group (AIG) number: 0151667001

Authorization status:

APPROVED

Authorization date:

2020-07-29

Patient Information leaflet

                                TULISSIN VIRBAC VERSION 17JULYE2020
OUTER LABEL
_ENGLISH_ MAIN PANEL
DIN XXXXXXXX
Pr
Tulissin
_TULATHROMYCIN INJECTION _
_STERILE _
Veterinary Use Only
Antibiotic
FOR CATTLE, SWINE AND SHEEP
WARNINGS: Treated animals must not be slaughtered for use in food for
at least 44 days in cattle, 8 days in swine
and 16 days in sheep, after the latest treatment with this drug. Do
not use in dairy cows 20 months of age and older.
To limit the development of antimicrobial resistance, TULISSIN should
only be used (1) as an arrival treatment in
feedlot calves when BRD has been diagnosed and calves are at high risk
of developing BRD, and (2) for control of
SRD outbreak when groups of pigs are at high risk of developing SRD.
KEEP OUT OF REACH OF CHILDREN.
NOTE: To reduce the possibility of excess trim at the injection site
it is recommended that swine not be slaughtered for
up to 35 days after the latest treatment with this drug.
_NET 20 ML/ 50 ML / 100 ML / 250 ML / 500 ML _
Lot:
EXP:
_ENGLISH_ SIDE PANEL
ACTIVE INGREDIENT: Tulathromycin, 100 mg/mL
PRESERVATIVE: Monothioglycerol, 5 mg/mL
INDICATIONS: _BEEF AND NON-LACTATING DAIRY CATTLE:_ For the treatment
of bovine respiratory_ _disease (BRD) and for
the reduction of_ _morbidity associated with BRD in feedlot calves_
_during the first 14 days in the feedlot when_ _
administered at the time of arrival. For the_ _treatment of infectious
bovine_ _keratoconjunctivitis (IBK). For the treatment
of_ _bovine foot rot (interdigital necrobacillosis)._ _
_SUCKLING CALVES, DAIRY CALVES, AND VEAL CALVES_: For the treatment of
BRD._ _
_SWINE:_ For the treatment of swine respiratory disease (SRD) and for
the control of SRD in groups of pigs where SRD
bas been diagnosed.
_SHEEP:_ For the treatment of foot rot.
See package insert for the complete list of bacteria susceptible to
tulathromycin in cattle, swine and sheep.
DOSAGE AND ADMINISTRATION: Administer in the neck by subcutaneous
injection in cattle and intramuscular injection
in swine and sheep, a single dose of 2.5 mg/kg body weight. Do 
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet French 29-07-2020

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