Ivermectin for Pigs
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Noromectin Injection for Cattle, Sheep & Pigs is a ready to use solution of ivermectin 10mg/mL, a broad-spectrum antiparasitic treatment for cattle, sheep & pigs
Indications
Kills adult and fourth-stage larvae of the gastrointestinal roundworms Ascaris sum, Hyostrongylus rubidus and Oesophagostomum spp. Kills the adult and and somatic larval stages of Strongyloides ransomi. Kills adult lungworms (Metastrongylus spp).
External Parasites Kills mange mites (Sarcoptes scabiei var suis).Noromectin Injection for Cattle, Sheep & Pigs is to be given to cattle, sheep and pigs by subcutaneous injection only. Standard injection equipment is suitable for administration. For pigs, use of a 18-gauge 12mm needle is recommended. Intramuscular injection will result in prolonged residues.
DOSE RATE: 1mL /33kg bodyweight
| Bodyweight | Dose Rate | Doses per 500ml |
| 17 - 33kg | 1.0ml | 500 |
| 34 - 50kg | 1.5ml | 333 |
| 51 - 66kg | 2.0ml | 250 |
| 67 - 99kg | 3.0ml | 166 |
| 100 -133kg | 4.0ml | 125 |
| 134 -166kg | 5.0ml | 100 |
| 167 -200kg | 6.0ml | 83 |
MEAT: Pigs producing meat or offal for human consumption must not be sold for slaughter either during treatment or within 28 days of the last treatment.
Where intramuscular injection may have occurred, cattle and sheep producing meat or offal for human consumption must not be sold for slaughter within 63 days of the last treatment (pigs).This product is not for intravenous or intramuscular use. Noromectin Injection for Cattle, Sheep & Pigs is a low-volume product registered for use in the stated species. It should not be used in other species as severe adverse reactions, including fatalities in dogs, may occur.
Pharmaceutical Precautions:
This product does not contain antimicrobial preservatives. Swab the cap with alcohol before each use. Use a dry, sterile needle and syringe or other injection equipment. Discard contents unused after 6 months from broaching the pack. Store below 25°C. Protect from direct sunlight.
Additional information:
Transitory discomfort has been noted following treatment in some cattle. A low incidence of soft tissue swelling at the injection site has been observed. These reactions disappear without treatment.
Registered pursuant to the ACVM Act 1997 No. A8208