KALAFEV, 50 mg/ml, ενέσιμο διάλυμα για βοοειδή, χοίρους και άλογα
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FLUNIXIN MEGLUMINE
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Valid
Authorised in these countries:
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Greece
Product identification
Medicine name:
KALAFEV, 50 mg/ml, ενέσιμο διάλυμα για βοοειδή, χοίρους και άλογα
Active substance and strength:
-
FLUNIXIN MEGLUMINE
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Authorisation number:
- 69428/18/26-11-2019/K-0186601
Product identification number:
- 54538d6f-84c8-4715-90d3-3e15b6421552
Permanent identification number:
- 600000096232
Product details
Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
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Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
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Meat and offal10day
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Milk24hour
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- Horse
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Meat and offal7day
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- Pig
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Meat and offal18day
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Intravenous use
- Cattle
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Meat and offal10day
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Milk24hour
-
- Horse
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Meat and offal7day
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- Pig
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Meat and offal18day
-
Availability
Package description:
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
- Available only in ελληνικά
Manufacturing sites for batch release:
- Fatro S.p.A.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.
Authorisation details
Authorisation status:
-
Valid
Authorisation procedure type:
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Marketing Authorisation
Procedure number:
- NA
Date of authorisation status change:
Legal basis of product authorisation:
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Generic (abridged application) - art 13(1)
Authorisation country:
-
Greece
Responsible authority:
- National Organization For Medicines
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation issued:
Reference member state:
This information is not available for this product.
Concerned member states:
This information is not available for this product.
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.
Additional information
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
First published:
Last updated:
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