Veterinary Medicines Information website

Nafpenzal DC, 300 mg + 100 mg + 100 mg/3g ενδομαστικό εναιώρημα για βοοειδή, πρόβατα και αίγες

Authorised
  • Nafcillin
  • Dihydrostreptomycin
  • Benzylpenicillin procaine
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Product identification

Medicine name:
Nafpenzal DC, 300 mg + 100 mg + 100 mg/3g ενδομαστικό εναιώρημα για βοοειδή, πρόβατα και αίγες
Active substance:
  • Nafcillin
  • Dihydrostreptomycin
  • Benzylpenicillin procaine
Target species:
  • Goat
  • Sheep
  • Cattle (dairy cow)
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Nafcillin
    100.00
    milligram(s)
    /
    1.00
    Syringe
  • Dihydrostreptomycin
    100.00
    milligram(s)
    /
    1.00
    Syringe
  • Benzylpenicillin procaine
    300.00
    milligram(s)
    /
    1.00
    Syringe
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Goat
      • Meat and offal
        35
        day
      • Milk
        9
        day
    • Sheep
      • Meat and offal
        35
        day
      • Milk
        5
        day
      • Milk
        90
        day
    • Cattle (dairy cow)
      • Meat and offal
        16
        day
      • Milk
        48
        hour
      • Milk
        44
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51RC23
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Cyprus
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • CY00072V
Date of authorisation status change:

Documents

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Published on: 17/08/2026
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