NOROMYCIN LA Solution

Pays: Canada

Langue: français

Source: Health Canada

Achète-le

Notice patient Notice patient (PIL)
15-01-2018

Ingrédients actifs:

Oxytétracycline (Dihydrate d'oxytétracycline)

Disponible depuis:

NORBROOK LABORATORIES LTD.

Dosage:

200MG

forme pharmaceutique:

Solution

Composition:

Oxytétracycline (Dihydrate d'oxytétracycline) 200MG

Mode d'administration:

Intramusculaire

Unités en paquet:

250ML/500ML

Type d'ordonnance:

Prescription

Groupe thérapeutique:

Bétails; Porcs

Descriptif du produit:

Numéro de groupe d'ingrédients actifs (GIA) :0105553001

Statut de autorisation:

APPROUVÉ

Date de l'autorisation:

2004-01-12

Notice patient

                                _NOROMYCIN LA_
Pr
SOLUTION INJECTABLE STÉRILE
D’OXYTÉTRACYCLINE (SOUS
FORME DE DIHYDRATE)
USAGE VÉTÉRINAIRE
SEULEMENT.
OXYTETRACYCLINE (AS
DIHYDRATE) STERILE
INJECTABLE SOLUTION
VETERINARY USE
ONLY.
A LONG ACTING BROAD
SPECTRUM ANTIBIOTIC.
ACTIVE INGREDIENT PER ML:
OXYTETRACYCLINE
(AS OXYTETRACYCLINE
DIHYDRATE BP) 200 MG
ANTIBIOTIQUE À LARGE SPECTRE
À ACTION PROLONGÉE.
I
NGRÉDIENT ACTIF PAR ML:
OXYTÉTRACYCLINE
(SOUS FORME DE DIHYDRATE
D'OXYTÉTRACYCLINE BP) 200 MG
INDICATIONS:
Treatment of infections in cattle and swine caused by Oxytetracycline
susceptible
bacteria. This product provides sustained antibiotic blood levels over
a 4 day period
in cattle and swine following a single treatment.
DOSAGE AND ADMINISTRATION:
For intramuscular administration in cattle and swine and subcutaneous
administration in cattle only.
Inject at a rate of 1 mL/10 kg bodyweight. See package insert for
complete
directions.
CAUTIONS:
Occasional hypersensitivity reactions (anaphylaxis) have been observed
following
the parenteral administration of oxytetracycline. In such cases
administer
epinephrine immediately. The safety of this product in pregnant
animals has not
been demonstrated.
WARNINGS:
_Intramuscular administration_: Treated cattle and swine must not be
slaughtered for
use in food for at least 21 days after the latest treatment with this
drug.
_Subcutaneous administration_: Treated cattle must not be slaughtered
for use in food
for at least 42 days after the latest treatment with this drug.
Do not use in lactating dairy cattle. Keep out of reach of children.
NOTE:
To avoid the possibility of excessive trim at the site of injection,
do not slaughter
cattle for at least 42 days after the latest treatment with this drug.
STORAGE:
Store below 25°C and protect from light.
Do not freeze.
See package insert for complete
product information.
DISTRIBUTED BY:
Kane Veterinary Supplies Ltd.
11204 - 186 Street,
Edmonton, AB
T5S 2W2
Patent number CA2194576
032154L06
INDICATIONS:
Traitement des infections chez les bovins et les po
                                
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