Paracox 8 oral suspension
Paracox 8 oral suspension
Authorised
- Eimeria acervulina, Live
- Eimeria maxima, Live
- Eimeria maxima, strain MFP, Live
- Eimeria maxima, strain MFP, Live
Product identification
Medicine name:
Paracox 8 oral suspension
Paracox 8
Active substance:
- Eimeria acervulina, Live
- Eimeria maxima, Live
- Eimeria maxima, strain MFP, Live
- Eimeria maxima, strain MFP, Live
Target species:
-
Chicken (chick)
Route of administration:
-
In drinking water use
-
In drinking water/milk use
-
Topical
Product details
Active substance and strength:
-
Eimeria acervulina, Live500.00unknown0.00millilitre(s)
-
Eimeria maxima, Live200.00unknown0.00millilitre(s)
-
Eimeria maxima, strain MFP, Live200.00unknown0.00millilitre(s)
-
Eimeria maxima, strain MFP, Live100.00unknown0.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
In drinking water use
- Chicken (chick)
-
Meat and offal0day
-
Egg0day
-
-
In drinking water/milk use
- Chicken (chick)
-
Meat and offal0day
-
Egg0day
-
-
Topical
- Chicken (chick)
-
Meat and offal0day
-
Egg0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AN
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- (ID2): 1 Box with 1 Vial (Polyethylenterephthalat Glycol-modifiziert) with 20 millilitre(s) (20 millilitre(s))
- (ID4): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 500 millilitre(s) (500 millilitre(s))
- (ID3): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s) (100 millilitre(s))
- (ID1): 1 Box with 1 Vial (Polyethylenterephthalat Glycol-modifiziert) with 4 millilitre(s) (4 millilitre(s))
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- MSD Animal Health UK Limited
- Merck Sharp & Dohme Animal Health S.L.
Responsible authority:
- PEI
Authorisation number:
- 483a/91
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0210/001
Concerned member states:
-
Austria
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 28/01/2022
German (PDF)
Published on: 11/02/2022
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