Veterinary Medicines

Novocillin LC 1000 mg intramammary suspension for lactating cow

Authorised
  • Oxacillin sodium monohydrate
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Product identification

Medicine name:
Novocillin LC 1000 mg intramammary suspension for lactating cow
Novocillin LC 1000 mg интрамамарна суспензия за крави в лактационен период
Active substance:
  • Oxacillin sodium monohydrate
Target species:
  • Cattle (dairy cow)
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Oxacillin sodium monohydrate
    1042.50
    milligram(s)
    /
    10.00
    gram(s)
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle (dairy cow)
      • Meat and offal
        6
        day
      • Milk
        144
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51CF04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Available in:
  • Bulgaria
Package description:
  • (ID3) 240 gram(s): Box (Cardboard) with 24 Applicator (Linear Low Density PolyEthylene) each with 10 gram(s)
  • (ID2) 200 gram(s): Box (Cardboard) with 20 Applicator (Linear Low Density PolyEthylene) each with 10 gram(s)
  • (ID1) 100 gram(s): Box (Cardboard) with 10 Applicator (Linear Low Density PolyEthylene) each with 10 gram(s)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Pharmanovo Veterinaerarzneimittel GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vet-Agro Trading Sp. z o.o.
  • Produlab Pharma B.V.
  • Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-3084
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0333/001
Concerned member states:
  • Austria
  • Bulgaria
  • Cyprus
  • Czechia
  • Estonia
  • France
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Lithuania
  • Poland
  • Portugal
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/07/2024
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/07/2024
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Combined File of all Documents

English (PDF)
Published on: 14/06/2024
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