Veterinary Medicines

ALCARUMIN

Authorised
  • Calcium hydroxide
  • ILLICIUM VERUM
  • Rhubarb
  • Magnesium oxide
  • Calcium carbonate
  • CINCHONA OFFICINALIS BARK
  • Cobaltous carbonate basic
  • Cyberlindnera jadinii
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Product identification

Medicine name:
ALCARUMIN
Active substance:
  • Calcium hydroxide
  • ILLICIUM VERUM
  • Rhubarb
  • Magnesium oxide
  • Calcium carbonate
  • CINCHONA OFFICINALIS BARK
  • Cobaltous carbonate basic
  • Cyberlindnera jadinii
Target species:
  • Cattle
  • Goat
  • Sheep
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Calcium hydroxide
    28.80
    milligram(s)
    /
    1.00
    gram(s)
  • ILLICIUM VERUM
    28.80
    milligram(s)
    /
    1.00
    gram(s)
  • Rhubarb
    14.40
    milligram(s)
    /
    1.00
    gram(s)
  • Magnesium oxide
    43.20
    milligram(s)
    /
    1.00
    gram(s)
  • Calcium carbonate
    247.80
    milligram(s)
    /
    1.00
    gram(s)
  • CINCHONA OFFICINALIS BARK
    28.80
    milligram(s)
    /
    1.00
    gram(s)
  • Cobaltous carbonate basic
    0.34
    milligram(s)
    /
    1.00
    gram(s)
  • Cyberlindnera jadinii
    288.20
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for oral suspension
Withdrawal period by route of administration:
  • In drinking water use
    • Cattle
      • Milk
        0
        day
    • Cattle
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA02AF02
Legal status of supply:
  • Veterinary medicinal product not 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:
  • Azienda Terapeutica Italiana A.T.I. S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.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

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Italian (PDF)
Published on: 3/06/2022
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