Veterinary Medicine Information website

VETAMPLIUS

Authorised
  • Ampicillin
  • Ampicillin
  • Ampicillin
  • Ampicillin
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Product identification

Medicine name:
VETAMPLIUS
Active substance:
  • Ampicillin
  • Ampicillin
  • Ampicillin
  • Ampicillin
Target species:
  • Cattle
  • Dog
  • Sheep
  • Cat
  • Pig
  • Horse
Route of administration:
  • Intraperitoneal use
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Ampicillin
    2.00
    gram(s)
    /
    1.00
    Bottle
  • Ampicillin
    4.00
    gram(s)
    /
    1.00
    Bottle
  • Ampicillin
    10.00
    gram(s)
    /
    1.00
    Bottle
  • Ampicillin
    100.00
    gram(s)
    /
    1.00
    Bottle
Pharmaceutical form:
  • Powder and solvent for solution for injection
Withdrawal period by route of administration:
  • Intraperitoneal use
    • Cattle
      • Meat and offal
        3
        day
      • Milk
        5
        day
    • Sheep
      • Meat and offal
        9
        day
      • Milk
        5
        day
    • Pig
      • Meat and offal
        9
        day
    • Horse
      • Meat and offal
        9
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        3
        day
      • Milk
        5
        day
    • Sheep
      • Meat and offal
        9
        day
      • Milk
        5
        day
    • Pig
      • Meat and offal
        9
        day
    • Horse
      • Meat and offal
        9
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        3
        day
      • Milk
        5
        day
    • Sheep
      • Meat and offal
        9
        day
      • Milk
        5
        day
    • Pig
      • Meat and offal
        9
        day
    • Horse
      • Meat and offal
        9
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
  • Bioquim S.A.
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 3/06/2022
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