Veterinary Medicines

AMOXICILINA FP 200 mg/ml, suspensie injectabilă pentru cai, bovine, oi, capre, porci, câini, pisici, găini

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
AMOXICILINA FP 200 mg/ml, suspensie injectabilă pentru cai, bovine, oi, capre, porci, câini, pisici, găini
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Cattle
  • Horse
  • Goat
  • Sheep
  • Pig
  • Cat
  • Dog
  • Chicken (broiler)
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        3
        day
    • Horse
      • Meat and offal
        21
        day
    • Goat
      • Meat and offal
        21
        day
      • Milk
        3
        day
    • Sheep
      • Meat and offal
        21
        day
      • Milk
        3
        day
    • Pig
      • Meat and offal
        21
        day
    • Cat
    • Dog
    • Chicken (broiler)
      • Meat and offal
        21
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        3
        day
    • Horse
      • Meat and offal
        21
        day
    • Goat
      • Meat and offal
        21
        day
      • Milk
        3
        day
    • Sheep
      • Meat and offal
        21
        day
      • Milk
        3
        day
    • Pig
      • Meat and offal
        21
        day
    • Cat
    • Dog
    • Chicken (broiler)
      • Meat and offal
        21
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Romania
Available in:
  • Romania
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
  • Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pasteur Filiala Filipesti S.A.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 140080
Date of authorisation status change:

Documents

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Romanian (PDF)
Published on: 12/12/2024
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