Authorised

Product identification

Medicine name:
Nafpenzal DC suspensija ievadīšanai tesmenī liellopiem
Active substance:
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
  • Nafcillin sodium
Target species:
  • Cattle (dry cow)
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Benzylpenicillin procaine
    300.00
    milligram(s)
    /
    1.00
    Syringe
  • Dihydrostreptomycin sulfate
    100.00
    milligram(s)
    /
    1.00
    Syringe
  • Nafcillin sodium
    100.00
    milligram(s)
    /
    1.00
    Syringe
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle (dry cow)
      • Meat and offal
        14
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51RC23
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • PVD
Authorisation number:
  • V/NRP/93/0034
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 5/03/2024

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 5/03/2024

Labelling

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 5/03/2024

Source URL: https://medicines.health.europa.eu/veterinary/600000006384