NAFPENZAL T POMMADE INTRAMAMMAIRE POUR VACHES BREBIS ET CHEVRES
NAFPENZAL T POMMADE INTRAMAMMAIRE POUR VACHES BREBIS ET CHEVRES
Authorised
- Nafcillin
- Dihydrostreptomycin
- Benzylpenicillin procaine monohydrate
Product identification
Medicine name:
NAFPENZAL T POMMADE INTRAMAMMAIRE POUR VACHES BREBIS ET CHEVRES
Active substance:
- Nafcillin
- Dihydrostreptomycin
- Benzylpenicillin procaine monohydrate
Target species:
-
Cattle (cow)
-
Sheep (ewe)
-
Goat (adult female)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Nafcillin100.00/milligram(s)1.00Syringe
-
Dihydrostreptomycin100.00/milligram(s)1.00Syringe
-
Benzylpenicillin procaine monohydrate300.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (cow)
-
Meat and offal14day
-
Milk48day47,5 jours après le traitement si la période de tarissement est inférieure à 46 jours.
-
Milk36hour36 heures après le vêlage si la période de tarissement est égale ou supérieure à 46 jours.
-
-
Sheep (ewe)
-
Meat and offal28day
-
Milk14day14 jours après agnelage pour une période de tarissement inférieure à 3 mois.
-
Milk6day6 jours après agnelage quand la période de tarissement est supérieure ou égale à 3 mois.
-
-
Goat (adult female)
-
Meat and offal28day
-
Milk14day14 jours après la mise bas quand la période de tarissement est inférieure à 40 jours.
-
Milk10day10 jours après la mise bas quand la période de tarissement est supérieure à 40 jours.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RC23
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Available in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/5170868 1/1990
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 23/04/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 23/04/2025
