Depomycine, vet. Stungulyf, dreifa Handa hrossum, nautgripum, svínum, sauðfé, hundum og köttum
Depomycine, vet. Stungulyf, dreifa Handa hrossum, nautgripum, svínum, sauðfé, hundum og köttum
Authorised
- Dihydrostreptomycin
- Benzylpenicillin procaine
Product identification
Medicine name:
Depomycine, vet. Stungulyf, dreifa Handa hrossum, nautgripum, svínum, sauðfé, hundum og köttum
Active substance:
- Dihydrostreptomycin
- Benzylpenicillin procaine
Target species:
-
Horse
-
Cattle
-
Pig
-
Sheep
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Dihydrostreptomycin200.00milligram(s)1.00millilitre(s)
-
Benzylpenicillin procaine200.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Horse
-
Meat and offal10000000dayDýralyfið má ekki gefa hrossum séu sláturafurðir nýttar til manneldis
-
- Cattle
-
Meat and offal60day
-
Milk3day
-
- Pig
-
Meat and offal60day
-
- Sheep
-
Meat and offal60day
-
Milk10000000dayDýralyfið má ekki gefa mjólkandi ám sé mjólkin nýtt til manneldis
-
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Iceland
Package description:
- Available only in Icelandic
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- 822858
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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