AviPro IBD Xtreme Lyophilisate for suspension
AviPro IBD Xtreme Lyophilisate for suspension
Authorised
- Infectious bursal disease virus, strain V217, Live
Product identification
Medicine name:
AviPro IBD Xtreme Lyophilisate for suspension
AviPro IBD Xtreme
Active substance:
- Infectious bursal disease virus, strain V217, Live
Target species:
-
Chicken
Route of administration:
-
Intraocular use
Product details
Active substance and strength:
-
Infectious bursal disease virus, strain V217, Live1000.0050% Embryo Infective Dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for use in drinking water
Withdrawal period by route of administration:
-
Intraocular use
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID9): 1 Box with 10 Bottle (Glass) with 5000 Dose (50000 Dose)
- (ID5): 1 Box with 1 Bottle (Glass) with 10000 Dose (10000 Dose)
- (ID10): 1 Box with 10 Bottle (Glass) with 10000 Dose (100000 Dose)
- (ID2): 1 Box with 1 Bottle (Glass) with 1000 Dose (1000 Dose)
- (ID8): 1 Box with 10 Bottle (Glass) with 2500 Dose (25000 Dose)
- (ID1): 1 Box with 1 Bottle (Glass) with 500 Dose (500 Dose)
- (ID6): 1 Box with 10 Bottle (Glass) with 500 Dose (5000 Dose)
- (ID4): 1 Box with 1 Bottle (Glass) with 5000 Dose (5000 Dose)
- (ID7): 1 Box with 10 Bottle (Glass) with 1000 Dose (10000 Dose)
- (ID3): 1 Box with 1 Bottle (Glass) with 2500 Dose (2500 Dose)
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:
- Lohmann Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lohmann Animal Health GmbH & Co. KG
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- PEI.V.03418.01.1
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0238/001
Concerned member states:
-
Cyprus
-
Greece
-
Hungary
-
Italy
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 7/11/2023
Updated on: 8/11/2023
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