ATRAVET 10 MG INJECTABLE SOLUTION

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

şimdi satın al

Aktif bileşen:

ACEPROMAZINE MALEATE

Mevcut itibaren:

BOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.

Doz:

10MG

Farmasötik formu:

SOLUTION

Kompozisyon:

ACEPROMAZINE MALEATE 10MG

Uygulama yolu:

INTRAMUSCULAR

Paketteki üniteler:

50 ML

Reçete türü:

OTC

Terapötik grubu:

CATTLE; SWINE (PIGS); GOATS; HORSES; CATS; SHEEP; DOGS

Ürün özeti:

Active ingredient group (AIG) number: 0106148001

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

2007-10-09

Bilgilendirme broşürü

                                REVISION. . . . . .
OPERATOR . . . . .
DATE . . . . . . . . .
ART # . . . . . . . .
BAYER # . . . . . .
PRODUCT . . . . . .
TYPE/SIZE. . . . .
TEMPLATE # . . .
DIMENSIONS . .
DIELINES
PDF. . . . . . . . . .
BOEHRINGER
INGELHEIM
3
hal
05Dec19
382001-01
87018563
Atravet Injectable
ECL/50 mL
674
4.5” x 1.4375”
120-300-434 4/10/14 R1
120-300-435 4/10/14 R1
05Dec19 hal
BLACK
PMS 285
PMS 109
B1A8
(L)
EXP.
04028691533788
DIN 00053023
VETERINARY USE ONLY
USAGE VÉTÉRINAIRE SEULEMENT
ATRAVET®
10 MG INJECTABLE
Acepromazine Maleate
Injection, USP
NET 50 ML/CONTENU NET 50 ML
Sterile/Stérile
ACTIVE INGREDIENT PER ML: Acepromazine maleate USP 10 mg
PRESERVATIVE: Benzyl alcohol 1% w/v
Refer to folded package insert attached to the container for complete
product information.
WARNINGS: Keep out of reach of children. Treated animals must not be
slaughtered for use in food for at least 7 days after the latest
treatment
with this drug. Milk taken from treated animals during treatment and
within 48 hours after the latest treatment must not be used as food.
Do not use in horses that are to be slaughtered for use in food.
INGRÉDIENT ACTIF PAR ML : Maléate d’acépromazine USP 10 mg
AGENT DE CONSERVATION : Alcool benzylique 1% p/v
Voir la notice jointe à ce contenant pour des renseignements complets
sur le produit.
MISES EN GARDE : Garder hors de la portée des enfants. Les animaux
traités ne doivent pas être abattus à des fins alimentaires dans un
délai d’au moins 7 jours après le dernier traitement avec ce
médicament. Le lait provenant des animaux traités qui est extrait
pendant le traitement et dans les 48 heures après l’administration
de la dernière dose ne doit pas être utilisé comme aliment. Ne pas
utiliser chez les chevaux devant être abattus à des fins
alimentaires.
12/05/2019 TLR
Acceptable
_BY CATHERINE BARNES AT 3:45 PM, DEC 16, 2019_
_BY ANDREW BERTOLINI AT 9:14 AM, DEC 19, 2019_
_BY NORMAND PLOURDE AT 8:11 AM, DEC 23, 2019_
DATE SUBMITTED: JANUARY 9, 2020 (BOEHRINGER INGELHEIM ANIMAL HEALTH
CANAD
                                
                                Belgenin tamamını okuyun
                                
                            

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