Tulathromycin Bioveta, 100mg/ml, Solution for injection
Tulathromycin Bioveta, 100mg/ml, Solution for injection
Authorised
- Tulathromycin
Product identification
Medicine name:
Tulathromycin Bioveta, 100mg/ml, Solution for injection
TULATHROMYCIN Bioveta 100 mg/ml injekčný roztok pre hovädzí dobytok, ošípané a ovce
Active substance:
- Tulathromycin
Target species:
-
Cattle
-
Pig
-
Sheep
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Tulathromycin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal22day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption.,
-
-
-
Intramuscular use
-
Pig
-
Meat and offal13day
-
-
Sheep
-
Meat and offal16day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption.,
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01FA94
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Glass Vial 1 x 50.0 millilitre(s)
- Glass Vial 1 x 100.0 millilitre(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/032/DC/25-S
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0190/001
Concerned member states:
-
Bulgaria
-
Estonia
-
Latvia
-
Lithuania
-
Poland
-
Romania
-
Slovakia
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 16/12/2025