- Application under evaluation
- CVMP opinion
- European Commission decision
Overview
The marketing authorisation for Meloxivet has been withdrawn at the request of the marketing authorisation holder.
Meloxivet : EPAR - Summary for the public
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Product information
Meloxivet : EPAR - Product Information
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Meloxivet : EPAR - All Authorised presentations
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Product details
- Name of medicine
- Meloxivet
- Active substance
- meloxicam
- International non-proprietary name (INN) or common name
- meloxicam
- Species
- Dogs
- Anatomical therapeutic chemical veterinary (ATCvet) code
- QM01AC06
Pharmacotherapeutic group
Musculo-skeletal systemTherapeutic indication
Alleviation of inflammation and pain in both acute and chronic musculoskeletal disorders.
Authorisation details
- EMA product number
- EMEA/V/C/000124
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.
- Marketing authorisation holder
- Eli Lilly and Company Limited
Eli Lilly and Company Limited
Elanco Animal Health,
Lilly House
Priestley Road
Basingstoke
RG24 9NL
United Kingdom - Marketing authorisation issued
- 14/11/2007
- Revision
- 5
Assessment history
Meloxivet : EPAR - Procedural steps taken and scientific information after authorisation
English (EN) (218.08 KB - PDF)
News on Meloxivet
More information on Meloxivet
Questions and answers on generic medicines
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italiano (IT) (67.62 KB - PDF)
latviešu valoda (LV) (111.81 KB - PDF)
lietuvių kalba (LT) (86.76 KB - PDF)
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Malti (MT) (89.35 KB - PDF)
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