MICOTIL Solution

Maa: Kanada

Kieli: ranska

Lähde: Health Canada

Aktiivinen ainesosa:

Tilmicosin

Saatavilla:

ELANCO CANADA LIMITED

Annos:

300MG

Lääkemuoto:

Solution

Koostumus:

Tilmicosin 300MG

Antoreitti:

Sous-cutanée

Kpl paketissa:

50/100/250ML

Prescription tyyppi:

Prescription

Terapeuttinen ryhmä:

Bétails; Mouton

Tuoteyhteenveto:

Numéro de groupe d'ingrédients actifs (GIA) :0121139001

Valtuutuksen tilan:

APPROUVÉ

Valtuutus päivämäärä:

2004-11-05

Pakkausseloste

Pr
Micotil™ 100 mL Carton Label
04Oct2022
PR
MICOTIL
TM
1
100 ML CARTON
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MAIN PANEL:
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AH0230
DIN 00857602
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PR
MICOTIL
TM
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Net 100 mL
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TILMICOSIN INJECTION USP
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VETERINARY USE ONLY
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STERILE
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Each mL contains 300 mg of tilmicosin. For subcutaneous use in cattle
and lambs only.
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Do not use in automatically powered syringes. See pull-out label for
important safety
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information.
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MEDICINAL INGREDIENT: tilmicosin
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NON-MEDICINAL INGREDIENTS: propylene glycol 25% w/v, phosphoric acid
and water for
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injection.
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WARNINGS:
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Treated cattle must not be slaughtered for use in food for at least 28
days after the
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latest treatment with this drug.
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Do not use in lactating dairy cattle.
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Treated sheep must not be slaughtered for use in food for at least 36
days after the
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latest treatment with this drug.
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HUMAN WARNINGS: NOT FOR HUMAN USE. HUMAN INJECTION HAS BEEN
ASSOCIATED WITH FATALITIES. DO NOT USE IN AUTOMATICALLY POWERED
SYRINGES.
EXERCISE EXTREME CAUTION TO AVOID ACCIDENTAL SELF-INJECTION. IN CASE
OF HUMAN
INJECTION, CONSULT A PHYSICIAN IMMEDIATELY AND APPLY ICE OR COLD PACK
TO
INJECTION SITE. DO NOT APPLY ICE DIRECTLY TO SKIN. FOR EMERGENCY
MEDICAL
INFORMATION CALL 1-855-281-1673.
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SEE PULL-OUT LABEL FOR NOTE TO PHYSICIAN.
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KEEP OUT OF REACH OF CHILDREN. AVOID CONTACT WITH EYES.
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Elanco
Canada Limited
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1919 Minnesota Court, Suite 401
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Mississauga, Ontario L5N 0C9
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Pr
Micotil™ 100 mL Carton Label
04Oct2022
RIGHT PANEL:
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INDICATIONS: For the treatment of bovine respiratory disease (BRD)
associated with
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_Mannheimia (Pasteurella) haemolytica_ and _Pasteurella multocida. _
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For the reduction of morbidity associated with bovine respiratory
disease (BRD) in
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feedlot calves, caused by _Mannheimia (Pasteurella) haemolytica_ and
_Pasteurella _
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_multocida_, during the first 30 days in the feedlot, when
administered at the time of
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arrival.
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For the treatment of pneumonic pasteurellosis in lambs associated with
_Mannheimia _
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