Riik: Austraalia
keel: inglise
Allikas: APVMA (Australian Pesticides and Veterinary Medicines Authority)
EGG DROP SYDROME 76 VIRUS STRAIN BC 14; NEWCASTLE DISEASE VIRUS CLONE 30
INTERVET AUSTRALIA PTY LIMITED
Newcastle disease virus (I)+vaccine - egg drop syndrome-
MISC. VACCINES OR ANTI SERA
EGG DROP SYDROME 76 VIRUS STRAIN BC 14 VACCINE-VIRAL Active 6.5 units; NEWCASTLE DISEASE VIRUS CLONE 30 VACCINE-VIRAL Active 50.0 units
*(1000; *doses); 500mL
VM - Veterinary Medicine
INTERVET AUSTRALIA
POULTRY | BREEDERS | BROILER | CHICKENS | CHICKS | CHOOKS | DAY OLD CHICKS | HATCHLINGS | LAYERS
IMMUNOTHERAPY
AVIAN HAEMAGGLUTINATING ADENOVIRUS | NEWCASTLE DISEASE | ADENOVIRUS | EGG DROP SYNDROME
Poison schedule: 0; Withholding period: Zero (0) days.; Host/pest details: POULTRY: [AVIAN HAEMAGGLUTINATING ADENOVIRUS, NEWCASTLE DISEASE]; Poison schedule: 0; Withholding period: WHP: As per the label Zero (0) days.; Host/pest details: POULTRY: [AVIAN HAEMAGGLUTINATING ADENOVIRUS, NEWCASTLE DISEASE]; Poison schedule: 0; Withholding period: WHP: NIL; Host/pest details: POULTRY: [AVIAN HAEMAGGLUTINATING ADENOVIRUS, NEWCASTLE DISEASE]; Poison schedule: 0; Withholding period: ; Host/pest details: POULTRY: [AVIAN HAEMAGGLUTINATING ADENOVIRUS, NEWCASTLE DISEASE]; For the vaccination of layers and breeders for the protection against sickness and death caused by Newcastle disease in early -mid lay and for the protection of layers and breeders against Egg Drop Syndrome '76.
Registered
2023-07-01
NOBILIS EDS + ND COMBINED INACTIVATED VACCINE AGAINST EDS'76 AND NEWCASTLE DISEASE 58494/133830 Product Name: APVMA Approval No: Label Name: NOBILIS EDS + ND COMBINED INACTIVATED VACCINE AGAINST EDS'76 AND NEWCASTLE DISEASE Signal Headings: FOR ANIMAL TREATMENT ONLY Constituent Statements: EDS’76 virus BC14: inducing ≥ 6.5 log2 HI units per dose; NDV Clone 30: inducing ≥ 4 log2 HI units per 1/50th dose or containing ≥ 50 PD50 units per dose, in oil adjuvant emulsion. Nobilis EDS+ND contains one immunogenic strain of Newcastle Disease virus and one immunogenic strain of EDS’76 virus. The viruses are inactivated with formalin. Subsequently they have been suspended in the aqueous phase of an oil adjuvant emulsion. Claims: The vaccine is recommended for the vaccination of layers and breeders for the protection against sickness and death caused by Newcastle disease in early-mid lay and for the protection of layers and breeders against Egg Drop Syndrome ’76. Net Contents: 500mL (1000 doses) Directions for Use: Restraints: Do not mix with other vaccines. Contraindications: Precautions: Vaccinate healthy birds only. Side Effects: Vaccination reactions: In healthy birds no clinical reaction to vaccination will be observed. For some weeks after vaccination a slight swelling may be felt at the site of vaccination. Local tissue reactions may occur. RLP APPROVED For Official Use Only Dosage and Administration: Shake the bottle well before and during use. Broached vials should be used within 3 hours. Before using vaccine allow it to reach an ambient temperature (15°C and 25°C). Use sterile injection equipment. Each bird should be given 0.5 mL of vaccine intramuscularly (IM) in the thigh or chest muscle or subcutaneously (SC) into the lower part of the neck. Recommended vaccination program: Nobilis EDS+ND should be given to birds around 14-18 weeks of age but not less than 4 weeks before the expected onset of lay. For an optimal booster effect, the birds must be primed with live vaccine against Newcastle Disease a Lugege kogu dokumenti
PRODUCT NAME: NOBILIS EDS + ND COMBINED INACTIVATED VACCINE AGAINST EDS 76 AND NEWCASTLE DISEASE MATERIAL SAFETY DATA SHEET THIS REVISION ISSUED: JULY, 2014 PAGE: 1 OF 6 MATERIAL SAFETY DATA SHEET Issued by: Intervet Australia Pty Limited (trading as MSD Animal Health) Phone: 1 800 033 461 (Business Hours) Poisons Information Centre: 13 11 26 from anywhere in Australia, (0800 764 766 in New Zealand) SUBSTANCE: Inactivated virus in an oil/water emulsion. TRADE NAME: NOBILIS ® EDS + ND COMBINED INACTIVATED VACCINE AGAINST EDS 76 AND NEWCASTLE DISEASE PRODUCT CODE: 27690 RECOMMENDED USE: Disease prevention by vaccination in laying and breeding poultry. APVMA NO: 58494 THIS VERSION ISSUED: Is valid for 5 years from this date. STATEMENT OF HAZARDOUS NATURE: THIS PRODUCT IS CLASSIFIED AS: Not classified as hazardous according to the criteria of SWA. Not a Dangerous Good according to the Australian Dangerous Goods (ADG) Code. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: S25. Avoid contact with eyes. SUSDP CLASSIFICATION: None allocated. ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated PHYSICAL DESCRIPTION & COLOUR: White emulsion. Presented in 500mL bottle. ODOUR: No odour. MAJOR HEALTH HAZARDS: no significant risk factors have been found for this product. The formaldehyde in this product is present at very low concentrations. However, persons with known sensitisation to formaldehyde should avoid contact with this product. INHALATION: SHORT TERM EXPOSURE: Available data indicates that this product is not harmful. However product may be mildly irritating, although unlikely to cause anything more than mild transient discomfort. LONG TERM EXPOSURE: No data for health effects associated with long term inhalation. POTENTIAL HEALTH EFFECTS EMERGENCY OVERVIEW SECTION 2 - HAZARDS IDENTIFICATION SECTION 1 - IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY ISSUED BY: INTERVET AUSTRALIA PTY LIMITED (TRADING AS MSD ANIMAL HEALTH) 91-105 HARPIN STREET TEL: 1 80 Lugege kogu dokumenti