October 2025 The European Medicines Agency (EMA) updated the regulatory documentation for Tulaven (tulathromycin), reflecting post-authorisation changes that support the continued availability of the veterinary antibiotic across European markets.
July 2025 Bioveta a.s. expanded its European tulathromycin portfolio after receiving marketing authorisations for its generic Tulathromycin Bioveta 100 mg/ml Solution for Injection, strengthening product availability across multiple EU countries.
January 2025 Bioveta a.s. received additional European marketing authorisations for its Tulathromycin Bioveta 100 mg/ml Solution for Injection, further expanding access to tulathromycin products in Central and Eastern Europe.