Veterinary Medicines

Nobilis MS Live, lyophilisate for oculonasal suspension for chickens

Not authorised
  • Mycoplasma synoviae, strain MS1, Live
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Product identification

Medicine name:
Nobilis MS Live, lyophilisate for oculonasal suspension for chickens
Nobilis MS Live lyofilisat til okulonasal suspension
Active substance:
  • Mycoplasma synoviae, strain MS1, Live
Target species:
  • Chicken
  • Chicken (for reproduction)
Route of administration:
  • Oculonasal use

Product details

Active substance and strength:
  • Mycoplasma synoviae, strain MS1, Live
    100.00
    million colony forming units
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for oculonasal suspension
Withdrawal period by route of administration:
  • Oculonasal use
    • Chicken
      • Egg
        0
        day
      • Meat and offal
        0
        day
    • Chicken (for reproduction)
      • Egg
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AE03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Denmark
Package description:
  • (ID6): 1 Box with 10 Bottle (Glass) with 2000 Dose (20000 Dose)
  • (ID5): 1 Box with 10 Bottle (Glass) with 1000 Dose (10000 Dose)
  • (ID4): 1 Box with 10 Bottle (Glass) with 500 Dose (5000 Dose)
  • (ID3): 1 Box with 1 Bottle (Glass) with 2000 Dose (2000 Dose)
  • (ID2): 1 Box with 1 Bottle (Glass) with 1000 Dose (1000 Dose)
  • (ID1): 1 Box with 1 Bottle (Glass) with 500 Dose (500 Dose)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 52158
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0260/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
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Danish (PDF)
Published on: 29/06/2023
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