Cyclospray 78.6 mg/g, cutaneous spray, suspension for pigs, sheep and cattle
Cyclospray 78.6 mg/g, cutaneous spray, suspension for pigs, sheep and cattle
Authorised
- CHLORTETRACYCLINE HYDROCHLORIDE
Product identification
Medicine name:
Cyclospray 78.6 mg/g, cutaneous spray, suspension for pigs, sheep and cattle
Cyclospray 78.6 mg/g, спрей за кожа, суспензия за говеда, овце и прасета
Active substance:
- CHLORTETRACYCLINE HYDROCHLORIDE
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
CHLORTETRACYCLINE HYDROCHLORIDE78.60milligram(s)1.00gram(s)
Pharmaceutical form:
-
Cutaneous spray, solution
Withdrawal period by route of administration:
-
Cutaneous use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
- Sheep
-
Meat and offal0day
-
Milk0hour
-
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- 520 ml (containing 261.52 g) pressurised container of coated tin plate with a plastic valve mechanism and spraying nozzle.
- 270 ml (containing 130.76 g) pressurised container of coated tin plate with a plastic valve mechanism and spraying nozzle.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Igs Aerosols GmbH
- Eurovet Animal Health B.V.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-3248
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0132/001
Concerned member states:
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
Iceland
-
Latvia
-
Romania
-
Slovakia
-
Slovenia
-
Sweden
-
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: 18/06/2024
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: 18/06/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 18/06/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/07/2024
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