HuveGuard MMAT
HuveGuard MMAT
Authorised
- Eimeria maxima, strain MCK +10, Live
- Eimeria mitis, strain Jormit 3+9, Live
- Eimeria acervulina, strain RA 3+20, Live
- Eimeria tenella, strain Rt 3+15, Live
Product identification
Medicine name:
HuveGuard MMAT
Huveguard MMAT Vet. suspension til oral suspension
Active substance:
- Eimeria maxima, strain MCK +10, Live
- Eimeria mitis, strain Jormit 3+9, Live
- Eimeria acervulina, strain RA 3+20, Live
- Eimeria tenella, strain Rt 3+15, Live
Target species:
-
Chicken
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Eimeria maxima, strain MCK +10, Live100.00unit(s)1.00Dose
-
Eimeria mitis, strain Jormit 3+9, Live100.00unit(s)1.00Dose
-
Eimeria acervulina, strain RA 3+20, Live50.00unit(s)1.00Dose
-
Eimeria tenella, strain Rt 3+15, Live150.00unit(s)1.00Dose
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
- Chicken
-
Meat and offal0day
-
Egg0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AN01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Available in:
-
Denmark
Package description:
- Low density polyethylene (LDPE) vial of 30 ml with a grey butyl rubber stopper and aluminum cap. Carboard box with 1 vial of 1000 doses.
- Low density polyethylene (LDPE) vial of 30 ml with a grey butyl rubber stopper and aluminum cap. Carboard box with 1 vial of 5000 doses.
- Low density polyethylene (LDPE) vial of 30 ml with a grey butyl rubber stopper and aluminum cap. Carboard box with 5 vials of 1000 doses.
- Low density polyethylene (LDPE) vial of 30 ml with a grey butyl rubber stopper and aluminum cap. Carboard box with 5 vials of 5000 doses.
- Low density polyethylene (LDPE) vial of 30 ml with a grey butyl rubber stopper and aluminum cap. Carboard box with 10 vials of 1000 doses.
- Low density polyethylene (LDPE) vial of 30 ml with a grey butyl rubber stopper and aluminum cap. Carboard box with 10 vials of 5000 doses.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet J.S.C.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 57384
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0206/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Malta
-
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
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Danish (, SUSPENSION TIL ORAL SUSPENSION)
Published on: 29/06/2023
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