Meloxidolor

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Authorised

This medicine is authorised for use in the European Union

meloxicam
MedicineVeterinaryAuthorised

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

Translate to Spanish | Important information about machine translation

  • 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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Latest procedure affecting product information:

български (BG) (93.36 KB - PDF)

Ver

español (ES) (81.97 KB - PDF)

Ver

čeština (CS) (93.99 KB - PDF)

Ver

dansk (DA) (83.34 KB - PDF)

Ver

Deutsch (DE) (82.76 KB - PDF)

Ver

eesti (ET) (82.18 KB - PDF)

Ver

ελληνικά (EL) (93.76 KB - PDF)

Ver

français (FR) (82.44 KB - PDF)

Ver

Gaeilge (GA) (83.57 KB - PDF)

Ver

hrvatski (HR) (92.27 KB - PDF)

Ver

italiano (IT) (82.29 KB - PDF)

Ver

latviešu (LV) (94.29 KB - PDF)

Ver

lietuvių (LT) (94.03 KB - PDF)

Ver

magyar (HU) (94.15 KB - PDF)

Ver

Malti (MT) (95.95 KB - PDF)

Ver

Nederlands (NL) (82.05 KB - PDF)

Ver

polski (PL) (95.62 KB - PDF)

Ver

português (PT) (83.01 KB - PDF)

Ver

română (RO) (94.17 KB - PDF)

Ver

slovenčina (SK) (94.08 KB - PDF)

Ver

slovenščina (SL) (82.27 KB - PDF)

Ver

suomi (FI) (81.54 KB - PDF)

Ver

svenska (SV) (82.05 KB - PDF)

Ver

Íslenska (IS) (83.29 KB - PDF)

Ver

norsk (NO) (82 KB - PDF)

Ver

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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