BioBos RCC, Suspension for injection
BioBos RCC, Suspension for injection
Authorised
- Bovine coronavirus, strain C-197, Inactivated
- Bovine rotavirus, strain TM-91, Inactivated
- Escherichia coli, serotype O8:K35 (fimbrial adhesin F5), Inactivated
Product identification
Medicine name:
BioBos RCC, injekcinė suspensija
BioBos RCC, Suspension for injection
Active substance:
- Bovine coronavirus, strain C-197, Inactivated
- Bovine rotavirus, strain TM-91, Inactivated
- Escherichia coli, serotype O8:K35 (fimbrial adhesin F5), Inactivated
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Bovine coronavirus, strain C-197, Inactivated1.00relative potency1.00Dose
-
Bovine rotavirus, strain TM-91, Inactivated1.00relative potency1.00Dose
-
Escherichia coli, serotype O8:K35 (fimbrial adhesin F5), Inactivated1.00relative potency1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AL01
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Glass Vial 20 x 1.0 Dose
- Glass Vial 10 x 1.0 Dose
- Glass Vial 2 x 1.0 Dose
- Plastic Vial 1 x 50.0 Dose
- Glass Vial 1 x 50.0 Dose
- Plastic Vial 24 x 25.0 Dose
- Glass Vial 24 x 25.0 Dose
- Plastic Vial 12 x 25.0 Dose
- Glass Vial 12 x 25.0 Dose
- Plastic Vial 1 x 25.0 Dose
- Glass Vial 1 x 25.0 Dose
- Plastic Vial 10 x 5.0 Dose
- Glass Vial 10 x 5.0 Dose
- Plastic Vial 5 x 5.0 Dose
- Glass Vial 5 x 5.0 Dose
- Plastic Vial 1 x 5.0 Dose
- Glass Vial 1 x 5.0 Dose
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:
- State Food And Veterinary Service
Authorisation number:
- LT/2/22/2718/001-010
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0176/001
Concerned member states:
-
Bulgaria
-
Croatia
-
Cyprus
-
Estonia
-
Hungary
-
Latvia
-
Lithuania
-
Malta
-
Poland
-
Romania
-
Slovakia
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.
Lithuanian (PDF)
Published on: 25/01/2023
PuAR Biobos RCC.pdf
English (PDF)
Download Published on: 29/08/2022
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