Veterinary Medicines

Noroclav 50 mg Tablets for Dogs and Cats

Authorised
  • Potassium clavulanate
  • Amoxicillin trihydrate
Download as PDF

Product identification

Medicine name:
Noroclav 50 mg Tablets for Dogs and Cats
Noroclav 50 mg Tablets for Dogs and Cats
Active substance:
  • Potassium clavulanate
  • Amoxicillin trihydrate
Target species:
  • Dog
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Potassium clavulanate
    11.91
    milligram(s)
    /
    1.00
    Tablet
  • Amoxicillin trihydrate
    45.92
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CR02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • The product is supplied in high-density polyethylene tubs with a polypropylene screw cap lid containing 100 tablets.
  • The product is supplied in high-density polyethylene tubs with a polyethylene screw cap lid containing 500 tablets.
  • The product is presented in packs containing 2 blister strips (aluminium-aluminium) each containing 10 tablets per strip
  • The product is presented in packs containing 10 blister strips (aluminium-aluminium) each containing 10 tablets per strip
  • The product is presented in packs containing 50 blister strips (aluminium-aluminium) each containing 10 tablets per strip

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Ltd
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/072/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0546/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • France
  • Luxembourg
  • Netherlands
  • Norway
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 2/03/2025
Download

Combined File of all Documents

English (PDF)
Published on: 2/03/2025
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."