Metaxx 20 mg/ml solution for injection for cattle, pigs and horses
Metaxx 20 mg/ml solution for injection for cattle, pigs and horses
Authorised
- Meloxicam
Product identification
Medicine name:
Metaxx 20 mg/ml solution for injection for cattle, pigs and horses
Metaxx 20 mg/ml ενέσιμο διάλυμα για βοοειδή, χοίρους και άλογα
Active substance:
- Meloxicam
Target species:
-
Cattle
-
Horse
-
Pig
Route of administration:
-
Subcutaneous use
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Meloxicam20.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offalno withdrawal periodmeat and offal 15 days
-
Milkno withdrawal period120 hours
-
-
Intravenous use
- Cattle
-
Meat and offalno withdrawal period15
-
Milkno withdrawal period120
-
- Horse
-
Meat and offalno withdrawal period5
-
-
Intramuscular use
- Pig
-
Meat and offalno withdrawal period5
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AC06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- Colourless glass (Type I) injection vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap. Cardboard box of 1 vial of 250 ml
- Colourless glass (Type I) injection vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap. Cardboard box of 1 vial of 100 ml
- Colourless glass (Type I) injection vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap. Cardboard box of 1 vial of 50 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic (abridged application) - art 13(1)
Marketing authorisation holder:
- Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Alfasan Nederland B.V.
- Produlab Pharma B.V.
Responsible authority:
- Ministry Of Agriculture Rural Development And Environment
Authorisation number:
- CY00885V
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0376/001/DC
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 17/05/2023
Greek (PDF)
Published on: 29/05/2023
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