PULMOTIL PREMIX DRUG PREMIX

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Aktīvā sastāvdaļa:

TILMICOSIN (TILMICOSIN PHOSPHATE)

Pieejams no:

ELANCO CANADA LIMITED

Deva:

200G

Zāļu forma:

DRUG PREMIX

Kompozīcija:

TILMICOSIN (TILMICOSIN PHOSPHATE) 200G

Ievadīšanas:

ORAL

Vienības iepakojumā:

10KG

Receptes veids:

Prescription

Ārstniecības grupa:

CATTLE; SWINE (PIGS); RABBITS

Produktu pārskats:

Active ingredient group (AIG) number: 0121139002

Autorizācija statuss:

APPROVED

Autorizācija datums:

2011-11-01

Lietošanas instrukcija

PRODUCT LABEL PROFILE
PULMOTIL PREMIX – 10KG
Pr
Pulmotil
TM
Premix Bag Label
13Nov2017
ELANCO™
AF0472
PR
PULMOTIL
TM PREMIX
TILMICOSIN
FOR VETERINARY USE ONLY
ANTIBIOTIC
NET WEIGHT 10 KG
DIN 02240124
PREMIX
FOR USE IN SWINE, FEEDLOT CATTLE AND RABBIT FEEDS ONLY
INDICATIONS:
1.
As an aid in reducing the severity of swine respiratory disease (SRD)
associated with
_Actinobacillus pleuropneumoniae _and _Pasteurella multocida_ when fed
to pigs approximately
7 days prior to anticipated disease outbreak.
1
2.
As an aid in reducing the severity of porcine polyserositis and
arthritis associated with
_Haemophilus parasuis_ (Glasser's Disease) when fed to pigs
approximately 7 days prior to
anticipated outbreak.
1
3.
For the reduction of bovine respiratory disease (BRD) morbidity
associated with _Mannheimia _
_haemolytica, Pasteurella multocida _and/or _Histophilus somni_ in
groups of feedlot beef cattle
experiencing an outbreak of BRD.
2
4.
For the reduction in severity of respiratory disease caused by
_Pasteurella multocida _in
rabbits.
Note: To promote responsible use and limit the development of
antimicrobial resistance,
use Pulmotil Premix only under the following conditions:
1
In swine when factors associated with outbreaks of SRD or Glasser’s
Disease (such as
herd health status, target pig population, herd management and
environmental factors, etc.)
have been carefully considered.
2
In feedlot beef cattle when:
1)
clinical BRD has been diagnosed in at least 10% of animals in the
group to be treated;
AND
2)
treatment is initiated within the first 45 days of arrival in the
feedlot; AND
3)
medication is limited to one single period of 14 consecutive days of
treatment.
IMPORTANT:
Must be thoroughly mixed in feeds before use.
ACTIVE DRUG INGREDIENT:
tilmicosin (as tilmicosin
phosphate)...........................................200 g per
kilogram
PRODUCT LABEL PROFILE
PULMOTIL PREMIX – 10KG
Pr
Pulmotil
TM
Premix Bag Label
13Nov2017
MIXING DIRECTIONS:
INDICATION 1:
Thoroughly mix 1.0 kg Pulmotil Premix into 999 kg no