FOSFOCARNITINA
FOSFOCARNITINA
Authorised
- DL-methionine
- L-ASPARTIC ACID
- Cyanocobalamin
- Lysine hydrochloride
- L-arginine hydrochloride
- L-THREONINE
- Phosphorylcolamine
- Propyl parahydroxybenzoate
- ACETYLCARNITINE
Product identification
Medicine name:
FOSFOCARNITINA
Active substance:
- DL-methionine
- L-ASPARTIC ACID
- Cyanocobalamin
- Lysine hydrochloride
- L-arginine hydrochloride
- L-THREONINE
- Phosphorylcolamine
- Propyl parahydroxybenzoate
- ACETYLCARNITINE
Target species:
-
Buffalo
-
Cattle
-
Goat
-
Sheep
-
Pig
-
Horse
-
Rabbit
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
DL-methionine1.50/gram(s)100.00millilitre(s)
-
L-ASPARTIC ACID2.70/gram(s)100.00millilitre(s)
-
Cyanocobalamin10.00/milligram(s)100.00millilitre(s)
-
Lysine hydrochloride3.00/gram(s)100.00millilitre(s)
-
L-arginine hydrochloride1.20/gram(s)100.00millilitre(s)
-
L-THREONINE1.00/gram(s)100.00millilitre(s)
-
Phosphorylcolamine6.00/gram(s)100.00millilitre(s)
-
Propyl parahydroxybenzoate0.02/gram(s)100.00millilitre(s)
-
ACETYLCARNITINE1.00/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Buffalo
-
Milk0day
-
Meat and offal0day
-
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
-
Intravenous use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Rabbit
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA16AA51
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available 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:
- Zoetis Italia S.r.l
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.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
Combined File of all Documents
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in another language below.
Italian (PDF)
Published on: 2/11/2024