Meloxidyl

RSS

Authorised

This medicine is authorised for use in the European Union

meloxicam
MedicineVeterinaryAuthorised

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

Translate to Lithuanian | 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)

Rodyti

hrvatski (HR) (91.56 KB - PDF)

Rodyti

italiano (IT) (81.76 KB - PDF)

Rodyti

latviešu (LV) (92.14 KB - PDF)

Rodyti

lietuvių (LT) (92.19 KB - PDF)

Rodyti

magyar (HU) (92.76 KB - PDF)

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Malti (MT) (93.86 KB - PDF)

Rodyti

Nederlands (NL) (81.15 KB - PDF)

Rodyti

polski (PL) (93.22 KB - PDF)

Rodyti

português (PT) (82.53 KB - PDF)

Rodyti

română (RO) (91.73 KB - PDF)

Rodyti

slovenčina (SK) (81.75 KB - PDF)

Rodyti

slovenščina (SL) (81.76 KB - PDF)

Rodyti

suomi (FI) (81.11 KB - PDF)

Rodyti

svenska (SV) (81.47 KB - PDF)

Rodyti

Íslenska (IS) (81.52 KB - PDF)

Rodyti

norsk (NO) (81.52 KB - PDF)

Rodyti

български (BG) (93.36 KB - PDF)

Rodyti

español (ES) (81.97 KB - PDF)

Rodyti

čeština (CS) (93.99 KB - PDF)

Rodyti

dansk (DA) (83.34 KB - PDF)

Rodyti

Deutsch (DE) (82.76 KB - PDF)

Rodyti

eesti (ET) (82.18 KB - PDF)

Rodyti

ελληνικά (EL) (93.76 KB - PDF)

Rodyti

français (FR) (82.44 KB - PDF)

Rodyti

Gaeilge (GA) (83.57 KB - PDF)

Rodyti

hrvatski (HR) (92.27 KB - PDF)

Rodyti

italiano (IT) (82.29 KB - PDF)

Rodyti

latviešu (LV) (94.29 KB - PDF)

Rodyti

lietuvių (LT) (94.03 KB - PDF)

Rodyti

magyar (HU) (94.15 KB - PDF)

Rodyti

Malti (MT) (95.95 KB - PDF)

Rodyti

Nederlands (NL) (82.05 KB - PDF)

Rodyti

polski (PL) (95.62 KB - PDF)

Rodyti

português (PT) (83.01 KB - PDF)

Rodyti

română (RO) (94.17 KB - PDF)

Rodyti

slovenčina (SK) (94.08 KB - PDF)

Rodyti

slovenščina (SL) (82.27 KB - PDF)

Rodyti

suomi (FI) (81.54 KB - PDF)

Rodyti

svenska (SV) (82.05 KB - PDF)

Rodyti

Íslenska (IS) (83.29 KB - PDF)

Rodyti

norsk (NO) (82 KB - PDF)

Rodyti

Product details

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

Pharmacotherapeutic group

Oxicams

Authorisation details

EMA product number
EMEA/V/C/000115

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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