Nafpenzal DC intramammárna suspenzia
Nafpenzal DC intramammárna suspenzia
Authorised
- Dihydrostreptomycin
- Nafcillin
- Benzylpenicillin procaine
Product identification
Medicine name:
Nafpenzal DC intramammárna suspenzia
Active substance:
- Dihydrostreptomycin
- Nafcillin
- Benzylpenicillin procaine
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Dihydrostreptomycin100.00/milligram(s)1.00Syringe
-
Nafcillin100.00/milligram(s)1.00Syringe
-
Benzylpenicillin procaine300000.00/international unit(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal14day
-
Milkno withdrawal period36 hours after calving. The product must be applied at least 42 days before calving. If the cow calves before the end of the 42-day period, the remaining days must be added to the 36-hour withdrawal period for milk. At the same time, in such a case, it is necessary to check the presence of residues in the milk.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RC23
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/330/92-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 11/11/2024
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