MYOTROFIL
MYOTROFIL
Authorised
- ADENOSINE PHOSPHATE, SODIUM SALT
- Carnitine hydrochloride
- Sodium selenite
- Magnesium aspartate tetrahydrate
- Potassium aspartate hemihydrate
- Heptaminol hydrochloride
Product identification
Medicine name:
MYOTROFIL
Active substance:
- ADENOSINE PHOSPHATE, SODIUM SALT
- Carnitine hydrochloride
- Sodium selenite
- Magnesium aspartate tetrahydrate
- Potassium aspartate hemihydrate
- Heptaminol hydrochloride
Target species:
-
Cattle
-
Dog
-
Sheep
-
Cat
-
Pig
-
Horse (food producing)
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
ADENOSINE PHOSPHATE, SODIUM SALT0.25/gram(s)100.00millilitre(s)
-
Carnitine hydrochloride0.20/gram(s)100.00millilitre(s)
-
Sodium selenite0.05/gram(s)100.00millilitre(s)
-
Magnesium aspartate tetrahydrate1.75/gram(s)100.00millilitre(s)
-
Potassium aspartate hemihydrate1.30/gram(s)100.00millilitre(s)
-
Heptaminol hydrochloride0.50/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk0hour
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Horse (food producing)
-
Milk0day
-
Meat and offal0day
-
-
-
Intravenous use
-
Cattle
-
Milk0hour
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Horse (food producing)
-
Milk0day
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Milk0hour
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Horse (food producing)
-
Milk0day
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA13A
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
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:
- Izo S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
- Izo S.r.l.
- Izo S.r.l.
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
MYOTROFIL.pdf
Italian (PDF)
Download Published on: 8/07/2022