Nuflor 40 mg/g Premix for Medicated Feeding Stuff for Swine

देश: आयरलैंड

भाषा: अंग्रेज़ी

स्रोत: HPRA (Health Products Regulatory Authority)

इसे खरीदें

सक्रिय संघटक:

Florfenicol

थमां उपलब्ध:

Intervet Ireland Limited

ए.टी.सी कोड:

QJ01BA90

INN (इंटरनेशनल नाम):

Florfenicol

डोज़:

40 milligram(s)/gram

फार्मास्यूटिकल फॉर्म:

Premix for medicated feeding stuff

प्रिस्क्रिप्शन प्रकार:

POM: Prescription Only Medicine as defined in relevant national legislation

चिकित्सीय समूह:

Pigs

चिकित्सीय क्षेत्र:

florfenicol

चिकित्सीय संकेत:

Antibacterial

प्राधिकरण का दर्जा:

Authorised

प्राधिकरण की तारीख:

2007-08-31

उत्पाद विशेषताएं

                                Health Products Regulatory Authority
27 February 2018
CRN000WK7
Page 1 of 7
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Nuflor 40 mg/g Premix for Medicated Feeding Stuff for Swine
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Composition per gram:
​
​
ACTIVE SUBSTANCE:
QUANTITY:
​
Florfenicol
​40 mg
​
EXCIPIENTS:
​
​
Propylene Glycol (E1520)
10 mg
​
Ground Limestone
​qs to 1 g
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Premix for medicated feeding stuff.
White to off-white, free flowing powder with red and/or black grains
dispersed
throughout.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Pigs (Fattening pigs).
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment and metaphylaxis of swine respiratory disease caused
by
_Pasteurella multocida _susceptible to florfenicol in infected herds.
The presence of the
disease in the herd must be established before the product is used.
4.3 CONTRAINDICATIONS
Do not administer to boars intended for breeding.
Do not use in case of hypersensivity to the active substance or any of
the excipients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Animals showing a decreased appetite and/or a poor general condition
should be
treated by the parenteral route.
Health Products Regulatory Authority
27 February 2018
CRN000WK7
Page 2 of 7
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS:
The product should be used in conjunction with susceptibility testing
and take into
account official and local policy relating to the use of
antimicrobials.
This premix is intended for the manufacturing of solid medicated feed
and cannot be
used as it is; the incorporation rate of the premix in feed cannot be
lower than 5
kg/ton.
This premix contains ground limestone, which can lead to a decrease in
food
consumption and to a phosphorus calcium imbalance in feed intake. Care
should
therefore be taken to consider the calcium content of the final
medicated feed.
Treatment should not exceed 5 days.
In a field clinical study, within a wee
                                
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