Meloxidolor

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Authorised

This medicine is authorised for use in the European Union

meloxicam
MedicineVeterinaryAuthorised

Dutch 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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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)

Bekijk

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)

Bekijk

română (RO) (91.73 kB - PDF)

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slovenčina (SK) (81.75 kB - PDF)

Bekijk

slovenščina (SL) (81.76 kB - PDF)

Bekijk

suomi (FI) (81.11 kB - PDF)

Bekijk

svenska (SV) (81.47 kB - PDF)

Bekijk

Íslenska (IS) (81.52 kB - PDF)

Bekijk

norsk (NO) (81.52 kB - PDF)

Bekijk
Latest procedure affecting product information:

български (BG) (93.36 kB - PDF)

Bekijk

español (ES) (81.97 kB - PDF)

Bekijk

čeština (CS) (93.99 kB - PDF)

Bekijk

dansk (DA) (83.34 kB - PDF)

Bekijk

Deutsch (DE) (82.76 kB - PDF)

Bekijk

eesti (ET) (82.18 kB - PDF)

Bekijk

ελληνικά (EL) (93.76 kB - PDF)

Bekijk

français (FR) (82.44 kB - PDF)

Bekijk

Gaeilge (GA) (83.57 kB - PDF)

Bekijk

hrvatski (HR) (92.27 kB - PDF)

Bekijk

italiano (IT) (82.29 kB - PDF)

Bekijk

latviešu (LV) (94.29 kB - PDF)

Bekijk

lietuvių (LT) (94.03 kB - PDF)

Bekijk

magyar (HU) (94.15 kB - PDF)

Bekijk

Malti (MT) (95.95 kB - PDF)

Bekijk

Nederlands (NL) (82.05 kB - PDF)

Bekijk

polski (PL) (95.62 kB - PDF)

Bekijk

português (PT) (83.01 kB - PDF)

Bekijk

română (RO) (94.17 kB - PDF)

Bekijk

slovenčina (SK) (94.08 kB - PDF)

Bekijk

slovenščina (SL) (82.27 kB - PDF)

Bekijk

suomi (FI) (81.54 kB - PDF)

Bekijk

svenska (SV) (82.05 kB - PDF)

Bekijk

Íslenska (IS) (83.29 kB - PDF)

Bekijk

norsk (NO) (82 kB - PDF)

Bekijk

Product details

Name of medicine
Meloxidolor
Active substance
meloxicam
International non-proprietary name (INN) or common name
meloxicam

Pharmacotherapeutic group

Oxicams

Authorisation details

EMA product number
EMEA/V/C/002590

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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