METABOLASE FORTE, solution for injection for cattle, sheep, swine, horses
METABOLASE FORTE, solution for injection for cattle, sheep, swine, horses
Authorised
- Acetylmethionine
- ALPHA-TOCOPHEROL
- Carnitine
- Cyanocobalamin
Product identification
Medicine name:
Metabolase Forte, ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, άλογα
METABOLASE FORTE, solution for injection for cattle, sheep, swine, horses
Active substance:
- Acetylmethionine
- ALPHA-TOCOPHEROL
- Carnitine
- Cyanocobalamin
Target species:
-
Cattle
-
Sheep
-
Horse
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Acetylmethionine200.00/milligram(s)1.00millilitre(s)
-
ALPHA-TOCOPHEROL30.00/milligram(s)1.00millilitre(s)
-
Carnitine50.00/milligram(s)1.00millilitre(s)
-
Cyanocobalamin0.20/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0dayΝα μην χρησιμοποιούνται οι μαστοί των ζώων που υποβάλλονται σε θεραπεία για ανθρώπινη κατανάλωση.
-
Milk0dayΜηδέν ώρες (μηδέν αρμέγματα) μετά τον τοκετό, εάν η περίοδος ξηρασίας είναι ίση ή μεγαλύτερη από 49 ημέρες,
49 ημέρες μετά τη θεραπεία εάν η περίοδος ξηρασίας είναι μικρότερη από 49 ημέρες.
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11JC
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Available in:
-
Cyprus
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (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.
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY00076V
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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Published on: 8/12/2022