Nafpenzal DC (300 mg + 100 mg + 100 mg)/3 g Maść dowymieniowa
Nafpenzal DC (300 mg + 100 mg + 100 mg)/3 g Maść dowymieniowa
Authorised
- Dihydrostreptomycin sulfate
- Nafcillin sodium monohydrate
- Benzylpenicillin procaine
Product identification
Medicine name:
Nafpenzal DC (300 mg + 100 mg + 100 mg)/3 g Maść dowymieniowa
Active substance:
- Dihydrostreptomycin sulfate
- Nafcillin sodium monohydrate
- Benzylpenicillin procaine
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Dihydrostreptomycin sulfate100.00milligram(s)3.00gram(s)
-
Nafcillin sodium monohydrate100.00milligram(s)3.00gram(s)
-
Benzylpenicillin procaine300.00milligram(s)1.00milligram(s)
Pharmaceutical form:
-
Intramammary ointment
Withdrawal period by route of administration:
-
Intramammary use
- Cattle
-
Meat and offal5week
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RC23
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a 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:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0688
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
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