Novocillin LC 1000 mg intramammary suspension for lactating cow
Novocillin LC 1000 mg intramammary suspension for lactating cow
Authorised
- Oxacillin sodium monohydrate
Product identification
Medicine name:
Novocillin LC 1000 mg intramammary suspension for lactating cow
Novocillin LC
Active substance:
- Oxacillin sodium monohydrate
Target species:
-
Cattle (dairy cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Oxacillin sodium monohydrate1042.50milligram(s)10.00gram(s)
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle (dairy cow)
-
Meat and offal6day
-
Milk144hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- (ID3) 240 gram(s): Box (Cardboard) with 24 Syringe (Polyethylen geringer Dichte, linear) each with 10 gram(s)
- (ID2) 200 gram(s): Box (Cardboard) with 20 Syringe (Polyethylen geringer Dichte, linear) each with 10 gram(s)
- (ID1) 100 gram(s): Box (Cardboard) with 10 Syringe (Polyethylen geringer Dichte, linear) each with 10 gram(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Pharmanovo Veterinaerarzneimittel GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Vet-Agro Trading Ltd
- Produlab Pharma B.V.
- Vet-Agro Sp. z o.o.
- Multi-Trade Company "Vet-Agro" Sp. z o.o.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402684.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0333/001
Concerned member states:
-
Austria
-
Bulgaria
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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