Utertab 2000 mg intrauterine tablet for cattle
Utertab 2000 mg intrauterine tablet for cattle
Authorised
- Tetracycline hydrochloride
Product identification
Medicine name:
Utertab 2000 mg intrauterine tablet for cattle
Utertab 2 000 mg вътрематочни таблетки за говеда
Active substance:
- Tetracycline hydrochloride
Target species:
-
Cattle (lactating cow)
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Tetracycline hydrochloride2000.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Intrauterine tablet
Withdrawal period by route of administration:
-
Intrauterine use
- Cattle (lactating cow)
-
Milk96hour
-
Meat and offal10day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- (ID9) 500 Intrauterine tablet: unspecified outer container with 100 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID8) 400 Intrauterine tablet: unspecified outer container with 80 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID7) 300 Intrauterine tablet: unspecified outer container with 60 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID6) 200 Intrauterine tablet: unspecified outer container with 40 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID5) 100 Intrauterine tablet: unspecified outer container with 20 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID4) 50 Intrauterine tablet: unspecified outer container with 10 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID3) 20 Intrauterine tablet: unspecified outer container with 4 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
- (ID2) 10 Intrauterine tablet: unspecified outer container with 2 Blister (PolyVinyl Chloride; PolyEthylene; PolyVinylidene Chloride; Aluminium) each with 5 Intrauterine tablet
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:
- Animedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Animedica GmbH
- Animedica Herstellungs GmbH
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2827
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0176/001
Concerned member states:
-
Bulgaria
-
Croatia
-
Hungary
-
Ireland
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
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.
Bulgarian (PDF)
Published on: 29/03/2022
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 8/03/2024
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