CRYOMAREX RISPENS
CRYOMAREX RISPENS
Not authorised
- Marek's disease virus, serotype 1, strain CVI-988 (Rispens), Live
Product identification
Medicine name:
CRYOMAREX RISPENS
Cryomarex Rispens, Suspenze a rozpouštědlo pro injekční suspenzi
Active substance:
- Marek's disease virus, serotype 1, strain CVI-988 (Rispens), Live
Target species:
-
Chicken (chick, for replacement)
-
Chicken (broiler)
-
Chicken (for reproduction)
-
Chicken (layer hen)
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Marek's disease virus, serotype 1, strain CVI-988 (Rispens), Live10000.00/plaque forming unit1.00Dose
Pharmaceutical form:
-
Concentrate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Chicken (chick, for replacement)
-
Meat and offal0day
-
- Chicken (broiler)
-
Meat and offal0day
-
- Chicken (for reproduction)
-
Meat and offal0day
-
- Chicken (layer hen)
-
Meat and offal0day
-
-
Subcutaneous use
- Chicken (chick, for replacement)
-
Meat and offal0day
-
- Chicken (broiler)
-
Meat and offal0day
-
- Chicken (for reproduction)
-
Meat and offal0day
-
- Chicken (layer hen)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Czechia
Package description:
- 6 ampoules of 2000 doses of frozen suspension and 1 bag of 2.400 ml of diluent
- 2 ampoules of 2000 doses of frozen suspension and 1 bag of 800 ml of diluent
- 1 ampoule of 2000 doses of frozen suspension and 1 bag of 400 ml of de diluent
- 9 ampoules of 1000 doses of frozen suspension and 1 bag of 1.800 ml of diluent
- 7 ampoules of 1000 doses of frozen suspension and 1 bag of 1.400 ml of diluent
- 6 ampoules of 1000 doses of frozen suspension and 1 bag of 1.200 ml of diluent
- 3 ampoules of 1000 doses of frozen suspension and 1 bag of 600 ml of diluent
- 2 ampoules of 1000 doses of frozen suspension and 1 bag of 400 ml of diluent
- 1 ampoule of 1000 doses of frozen suspension + 1 bag of 200 ml of diluent
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:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/051/14-C
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0216/001
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: 12/04/2023
Czech (PDF)
Published on: 25/10/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 25/10/2022
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