Tulinovet

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Authorised

This medicine is authorised for use in the European Union

tulathromycin
MedicineVeterinaryAuthorised

Italian is available via eTranslation, the European Commission's machine translation service.

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  • Application under evaluation
  • CVMP opinion
  • European Commission decision

Overview

Up-to-date information on this veterinary medicinal product is available on the Veterinary Medicines Information website

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español (ES) (81.97 KB - PDF)

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čeština (CS) (93.99 KB - PDF)

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dansk (DA) (83.34 KB - PDF)

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Deutsch (DE) (82.76 KB - PDF)

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eesti (ET) (82.18 KB - PDF)

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ελληνικά (EL) (93.76 KB - PDF)

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français (FR) (82.44 KB - PDF)

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Gaeilge (GA) (83.57 KB - PDF)

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hrvatski (HR) (92.27 KB - PDF)

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italiano (IT) (82.29 KB - PDF)

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latviešu (LV) (94.29 KB - PDF)

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lietuvių (LT) (94.03 KB - PDF)

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magyar (HU) (94.15 KB - PDF)

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Malti (MT) (95.95 KB - PDF)

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Nederlands (NL) (82.05 KB - PDF)

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polski (PL) (95.62 KB - PDF)

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português (PT) (83.01 KB - PDF)

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română (RO) (94.17 KB - PDF)

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slovenčina (SK) (94.08 KB - PDF)

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slovenščina (SL) (82.27 KB - PDF)

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suomi (FI) (81.54 KB - PDF)

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svenska (SV) (82.05 KB - PDF)

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Íslenska (IS) (83.29 KB - PDF)

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norsk (NO) (82 KB - PDF)

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Product information

български (BG) (91.78 KB - PDF)

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español (ES) (81.51 KB - PDF)

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čeština (CS) (92.48 KB - PDF)

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dansk (DA) (82.05 KB - PDF)

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Deutsch (DE) (81.72 KB - PDF)

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eesti (ET) (81.22 KB - PDF)

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ελληνικά (EL) (91.79 KB - PDF)

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français (FR) (81.63 KB - PDF)

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Gaeilge (GA) (81.36 KB - PDF)

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hrvatski (HR) (91.56 KB - PDF)

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italiano (IT) (81.76 KB - PDF)

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latviešu (LV) (92.14 KB - PDF)

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lietuvių (LT) (92.19 KB - PDF)

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magyar (HU) (92.76 KB - PDF)

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Malti (MT) (93.86 KB - PDF)

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Nederlands (NL) (81.15 KB - PDF)

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polski (PL) (93.22 KB - PDF)

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português (PT) (82.53 KB - PDF)

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română (RO) (91.73 KB - PDF)

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slovenčina (SK) (81.75 KB - PDF)

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slovenščina (SL) (81.76 KB - PDF)

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suomi (FI) (81.11 KB - PDF)

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svenska (SV) (81.47 KB - PDF)

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Íslenska (IS) (81.52 KB - PDF)

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norsk (NO) (81.52 KB - PDF)

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български (BG) (93.36 KB - PDF)

Visualizza

español (ES) (81.97 KB - PDF)

Visualizza

čeština (CS) (93.99 KB - PDF)

Visualizza

dansk (DA) (83.34 KB - PDF)

Visualizza

Deutsch (DE) (82.76 KB - PDF)

Visualizza

eesti (ET) (82.18 KB - PDF)

Visualizza

ελληνικά (EL) (93.76 KB - PDF)

Visualizza

français (FR) (82.44 KB - PDF)

Visualizza

Gaeilge (GA) (83.57 KB - PDF)

Visualizza

hrvatski (HR) (92.27 KB - PDF)

Visualizza

italiano (IT) (82.29 KB - PDF)

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latviešu (LV) (94.29 KB - PDF)

Visualizza

lietuvių (LT) (94.03 KB - PDF)

Visualizza

magyar (HU) (94.15 KB - PDF)

Visualizza

Malti (MT) (95.95 KB - PDF)

Visualizza

Nederlands (NL) (82.05 KB - PDF)

Visualizza

polski (PL) (95.62 KB - PDF)

Visualizza

português (PT) (83.01 KB - PDF)

Visualizza

română (RO) (94.17 KB - PDF)

Visualizza

slovenčina (SK) (94.08 KB - PDF)

Visualizza

slovenščina (SL) (82.27 KB - PDF)

Visualizza

suomi (FI) (81.54 KB - PDF)

Visualizza

svenska (SV) (82.05 KB - PDF)

Visualizza

Íslenska (IS) (83.29 KB - PDF)

Visualizza

norsk (NO) (82 KB - PDF)

Visualizza

Product details

Name of medicine
Tulinovet
Active substance
tulathromycin
International non-proprietary name (INN) or common name
tulathromycin

Pharmacotherapeutic group

  • Antibacterials for systemic use
  • Macrolides

Authorisation details

EMA product number
EMEA/V/C/005076

Generic

This is a generic medicine, which is developed to be the same as a medicine that has already been authorised, called the reference medicine. A generic medicine contains the same active substance(s) as the reference medicine, and is used at the same dose(s) to treat the same disease(s). For more information, see Generic and hybrid medicines.

Assessment history

This page was last updated on

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