Moxisolv LA 100 mg/ml Solution for Injection for Cattle
  • Moxidectin
  • Valid
Authorised in these countries:
  • European Union
  • Slovakia
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Product identification

Medicine name:
Moxisolv LA 100 mg/ml Solution for Injection for Cattle
Moxisolv LA 100 mg/ml injekčný roztok pre hovädzí dobytok
Active substance and strength:
  • Moxidectin
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AB02
Authorisation number:
  • 96/006/DC/23-S
Product identification number:
  • 5560fa84-4733-4414-a95b-bfd32814a41a
Permanent identification number:
  • 600000106653

Product details

Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        108
        day
      • Milk
        no withdrawal period

Availability

Package description:
  • Carton box with 1 bottle containing 200 ml of product.
  • Carton box with 1 bottle containing 50 ml of product.
Manufacturing sites for batch release:
  • Bimeda Animal Health Limited
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • ES/V/0413/001
Date of authorisation status change:
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Authorisation country:
  • Slovakia
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Marketing authorisation holder:
  • Bimeda Animal Health Limited
Marketing authorisation issued:
Reference member state:
  • Spain
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Estonia
  • France
  • Germany
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Slovakia
  • United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

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

Documents

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