Nafpenzal DC 100 mg suspension intramammaire
Nafpenzal DC 100 mg suspension intramammaire
Authorised
- Nafcillin sodium
- Dihydrostreptomycin sulfate
- Benzylpenicillin procaine
Product identification
Medicine name:
Nafpenzal DC 100 mg suspension intramammaire
Nafpenzal DC 100 mg Suspension zur intramammären Anwendung
Active substance:
- Nafcillin sodium
- Dihydrostreptomycin sulfate
- Benzylpenicillin procaine
Target species:
-
Cattle (dairy cattle)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Nafcillin sodium100.00/milligram(s)1.00Syringe
-
Dihydrostreptomycin sulfate100.00/milligram(s)1.00Syringe
-
Benzylpenicillin procaine300.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dairy cattle)
-
Meat and offal5day
-
Milkno withdrawal periodTreatment to calving interval ≥ 46 days: 48 hours; Treatment to calving interval < 46 days: 46 days after treatment
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RC23
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Package description:
- 20 Intramammary syringes with 3g of Intramammary suspension
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (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 GmbH
Responsible authority:
- Ministry Of Health
Authorisation number:
- V 817/02/11/0746
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
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French (PDF)
Published on: 14/08/2023