Veterinary Medicines

Metacam 5 mg/ml - Solution for injection (cattle, pigs)

Authorised

Meloxicam

Download as PDF

Product identification

Medicine name:

Metacam 5 mg/ml - Solution for injection (cattle, pigs)

Active substance:

Meloxicam

Target species:

Cattle
Pig

Route of administration:

Intramuscular use
Intravenous use
Subcutaneous use

Product details

Active substance and strength:

Meloxicam

Presentation_strength:5 mg Reference:BP Index:0

Pharmaceutical form:

Solution for injection

Withdrawal period by route of administration:

Intramuscular use
- Cattle
  - Meat and offal
    
    15
    
    day
    
    15 days
- Pig
  - Meat and offal
    
    5
    
    day
    
    5 days
Intravenous use
- Cattle
  - Meat and offal
    
    15
    
    day
    
    15 days
- Pig
  - Meat and offal
    
    5
    
    day
    
    5 days
Subcutaneous use
- Cattle
  - Meat and offal
    
    15
    
    day
    
    15 days
- Pig
  - Meat and offal
    
    5
    
    day
    
    5 days

Anatomical therapeutic chemical veterinary (ATCvet) codes:

QM01AC06

Legal status of supply:

Veterinary medicinal product subject to veterinary prescription

Authorisation status:

Valid

Authorised in:

Package description:

Packaging:Injection vial (glass), Package_size:12 vials, Content:50 ml
Packaging:Injection vial (glass), Package_size:1 vial, Content:50 ml
Packaging:Injection vial (glass), Package_size:12 vials, Content:20 ml
Packaging:Injection vial (glass), Package_size:1 vial, Content:20 ml
Packaging:Injection vial (glass), Package_size:12 vials, Content:100 ml
Packaging:Injection vial (glass), Package_size:1 vial, Content:100 ml

Additional information

Entitlement type:

Marketing Authorisation

Legal basis of product authorisation:

Complete application (stand-alone) - Council Directive 81/851/EEC

Marketing authorisation holder:

Boehringer Ingelheim Vetmedica GmbH

Marketing authorisation date:

7/01/1998

Manufacturing sites for batch release:

Labiana Life Sciences S.A.

Responsible authority:

European Commission

Authorisation number:

This information is not available for this product.

Date of authorisation status change:

12/01/2010

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Combined File of all Documents

English (PDF)

Published on: 5/12/2024

Other languages (24)

Bulgarian (PDF)

Published on: 5/12/2024

Croatian (PDF)

Published on: 5/12/2024

Czech (PDF)

Published on: 5/12/2024

Danish (PDF)

Published on: 5/12/2024

Dutch (PDF)

Published on: 5/12/2024

Estonian (PDF)

Published on: 5/12/2024

Finnish (PDF)

Published on: 5/12/2024

French (PDF)

Published on: 5/12/2024

German (PDF)

Published on: 5/12/2024

Greek (PDF)

Published on: 5/12/2024

Hungarian (PDF)

Published on: 5/12/2024

Icelandic (PDF)

Published on: 5/12/2024

Italian (PDF)

Published on: 5/12/2024

Latvian (PDF)

Published on: 5/12/2024

Lithuanian (PDF)

Published on: 5/12/2024

Maltese (PDF)

Published on: 5/12/2024

Norwegian (PDF)

Published on: 5/12/2024

Polish (PDF)

Published on: 5/12/2024

Portuguese (PDF)

Published on: 5/12/2024

Romanian (PDF)

Published on: 5/12/2024

Slovak (PDF)

Published on: 5/12/2024

Slovenian (PDF)

Published on: 5/12/2024

Spanish (PDF)

Published on: 5/12/2024

Swedish (PDF)

Published on: 5/12/2024

ema-puar-v33-metacam-vra0151g-en.pdf

English (PDF)

Published on: 23/05/2024

ema-puar-metacam-v-033-par-en.pdf

English (PDF)

Published on: 17/03/2023

ema-puar-metacam-v-033-var-x-0107-en.pdf

English (PDF)

Published on: 17/03/2023

ema-puar-metacam-novem-var-ws-0264-en.pdf

English (PDF)

Published on: 17/03/2023

ema-puar-metacam-v-033-var-ii-0127-en.pdf

English (PDF)

Published on: 17/03/2023

ema-puar-metacam-v-033-var-x-0119-en.pdf

English (PDF)

Published on: 15/03/2023

How useful was this page?: