ROKOVAC NEO, injekcinė emulsija kiaulėms
ROKOVAC NEO, injekcinė emulsija kiaulėms
Authorised
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
- Escherichia coli, serotype O149:K88 (fimbrial adhesin F4ac), Inactivated
- Escherichia coli, serotype O147:K88 (fimbrial adhesin F4), Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Porcine rotavirus A, strain OSU 6, Inactivated
Product identification
Medicine name:
ROKOVAC NEO, injekcinė emulsija kiaulėms
Active substance:
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
- Escherichia coli, serotype O149:K88 (fimbrial adhesin F4ac), Inactivated
- Escherichia coli, serotype O147:K88 (fimbrial adhesin F4), Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Porcine rotavirus A, strain OSU 6, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated54000000000.00/Colony forming unit1.00Dose
-
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated54000000000.00/Colony forming unit1.00Dose
-
Escherichia coli, serotype O149:K88 (fimbrial adhesin F4ac), Inactivated54000000000.00/Colony forming unit1.00Dose
-
Escherichia coli, serotype O147:K88 (fimbrial adhesin F4), Inactivated54000000000.00/Colony forming unit1.00Dose
-
Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated54000000000.00/Colony forming unit1.00Dose
-
Porcine rotavirus A, strain OSU 6, Inactivated1000000.00/50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AL02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 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/2/11/2078/001-005
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 22/12/2025