Veterinary Medicines

Luminal vet, 100 mg tablets for dogs

Authorised
  • Phenobarbital
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Product identification

Medicine name:
Luminal vet, 100 mg tablets for dogs
Epirepress 100 mg Tablet
Epirepress 100 mg Comprimé
Epirepress 100 mg Tablette
Active substance:
  • Phenobarbital
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Phenobarbital
    100.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN03AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • (ID7) 120 Tablet: unspecified outer container with 1 Container (High Density PolyEthylene) with 120 Tablet
  • (ID6) 100 Tablet: unspecified outer container with 1 Container (High Density PolyEthylene) with 100 Tablet
  • (ID5) 60 Tablet: unspecified outer container with 1 Container (High Density PolyEthylene) with 60 Tablet
  • (ID4) 50 Tablet: unspecified outer container with 1 Container (High Density PolyEthylene) with 50 Tablet
  • (ID3) 180 Tablet: unspecified outer container with 6 Bottle (Glass) each with 30 Tablet
  • (ID2) 90 Tablet: unspecified outer container with 3 Bottle (Glass) each with 30 Tablet
  • (ID1) 30 Tablet: unspecified outer container with 1 Bottle (Glass) with 30 Tablet

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Desitin Arzneimittel GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Desitin Arzneimittel GmbH
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0141/002
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • Netherlands
  • Portugal
  • Spain
  • Sweden

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
Download
French (PDF)
Published on: 22/03/2022
Download
German (PDF)
Published on: 22/03/2022
Download
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