CLOTEAN injekčná suspenzia pre kone, hovädzí dobytok, ošípané, ovce, kozy, psi, mačky
CLOTEAN injekčná suspenzia pre kone, hovädzí dobytok, ošípané, ovce, kozy, psi, mačky
Authorised
- Clostridium tetani, antitoxin
Product identification
Medicine name:
CLOTEAN injekčná suspenzia pre kone, hovädzí dobytok, ošípané, ovce, kozy, psi, mačky
Active substance:
- Clostridium tetani, antitoxin
Target species:
-
Horse
-
Cattle
-
Pig
-
Sheep
-
Goat
-
Dog
-
Cat
Route of administration:
-
Cutaneous use
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Clostridium tetani, antitoxin300.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Cutaneous use
- Horse
-
All relevant tissues0day
-
- Cattle
-
Adipose tissue0day
-
- Pig
-
All relevant tissues0day
-
- Sheep
-
All relevant tissues0day
-
- Goat
-
All relevant tissues0day
-
- Dog
-
Not applicable0day
-
- Cat
-
All relevant tissues0day
-
-
Intravenous use
- Horse
-
All relevant tissues0day
-
- Cattle
-
All relevant tissues0day
-
- Pig
-
All relevant tissues0day
-
- Sheep
-
All relevant tissues0day
-
- Goat
-
All relevant tissues0day
-
- Dog
-
Not applicable0day
-
- Cat
-
Not applicable0day
-
-
Intramuscular use
- Horse
-
All relevant tissues0day
-
- Cattle
-
All relevant tissues0day
-
- Pig
-
All relevant tissues0day
-
- Sheep
-
All relevant tissues0day
-
- Goat
-
All relevant tissues0day
-
- Dog
-
Not applicable0day
-
- Cat
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AM
- QI03AM
- QI04AM02
- QI05AM01
- QI06AM
- QI07AM
- QI09AM04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- USKVBL
Authorisation number:
- 97/295/92-S
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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Slovak (PDF)
Published on: 7/01/2022
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