Ubroseal blue Dry Cow 2.6 g intramammary suspension for cattle
Ubroseal blue Dry Cow 2.6 g intramammary suspension for cattle
Authorised
- Bismuth subnitrate, heavy
Product identification
Medicine name:
Ubroseal blue Dry Cow 2.6 g intramammary suspension for cattle
UBROSEAL BLUE DRY COW
Active substance:
- Bismuth subnitrate, heavy
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Bismuth subnitrate, heavy2.60gram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG52X
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- A 4g polyethylene intramammary syringe consisting of a barrel with plunger and a polyethylene dual-cap.Cardboard box of 20 syringes and 20 cleaning towels
- A 4g polyethylene intramammary syringe consisting of a barrel with plunger and a polyethylene dual-cap.Polyethylene bucket of 60 syringes and 60 cleaning towels
- A 4g polyethylene intramammary syringe consisting of a barrel with plunger and a polyethylene dual-cap.Polyethylene bucket of 120 syringes and 120 cleaning towels
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:
- Univet Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Univet Limited
Responsible authority:
- Ministry Of Health
Authorisation number:
- 105111
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0437/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Liechtenstein
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
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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Italian (PDF)
Published on: 24/11/2023
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