Colosan, oplossing voor oraal gebruik
Colosan, oplossing voor oraal gebruik
Authorised
- FOENICULI AMARI FRUCTUS AETHEROLEUM
- LINSEED OIL
- ANISE OIL
- CARAWAY OIL
- COD-LIVER OIL
- CINNAMON OIL
- Sulfur
- MATRICARIAE AETHEROLEUM
Product identification
Medicine name:
Colosan, oplossing voor oraal gebruik
Active substance:
- FOENICULI AMARI FRUCTUS AETHEROLEUM
- LINSEED OIL
- ANISE OIL
- CARAWAY OIL
- COD-LIVER OIL
- CINNAMON OIL
- Sulfur
- MATRICARIAE AETHEROLEUM
Target species:
-
Cattle
-
Goat (adult female)
-
Sheep
-
Horse
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
FOENICULI AMARI FRUCTUS AETHEROLEUM0.01/millilitre(s)1.00millilitre(s)
-
LINSEED OIL0.75/millilitre(s)1.00millilitre(s)
-
ANISE OIL0.01/millilitre(s)1.00millilitre(s)
-
CARAWAY OIL0.01/millilitre(s)1.00millilitre(s)
-
COD-LIVER OIL0.18/millilitre(s)1.00millilitre(s)
-
CINNAMON OIL0.02/millilitre(s)1.00millilitre(s)
-
Sulfur0.03/gram(s)1.00millilitre(s)
-
MATRICARIAE AETHEROLEUM0.00/gram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Milkno withdrawal periodzero days
-
Meat and offalno withdrawal periodzero days
-
-
Goat (adult female)
-
Milkno withdrawal periodzero days
-
Meat and offalno withdrawal periodzero days
-
-
Sheep
-
Milkno withdrawal periodzero days
-
Meat and offalno withdrawal periodzero days
-
-
Horse
-
Meat and offalno withdrawal periodzero days
-
-
Pig
-
Meat and offalno withdrawal periodzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA03AX
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Available in:
-
Netherlands
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- SaluVet GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- SaluVet GmbH
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 5633
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Dutch (PDF)
Published on: 18/12/2024
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