DECTOSPOT 10 MG/ML POUR-ON SOLUTION FOR CATTLE AND SHEEP
DECTOSPOT 10 MG/ML POUR-ON SOLUTION FOR CATTLE AND SHEEP
Not authorised
- Deltamethrin
Product identification
Medicine name:
DECTOSPOT 10 MG/ML POUR-ON SOLUTION FOR CATTLE AND SHEEP
Dectospot 10 mg/ml šķīdums uzliešanai uz muguras liellopiem un aitām
Active substance:
- Deltamethrin
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Deltamethrin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Cattle
-
Meat and offal18day
-
Milk0day
-
-
Sheep
-
Meat and offal35day
-
Milk24hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AC11
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Latvia
Package description:
- 500 ml high density polyethylene flexipacks with twin neck dispenser, internal graduated calibration chamber and polypropylene heat-sealed screw cap.
- 1 litre high-density polyethylene flat bottom containers with polypropylene closures and tamper evident with induction heat-sealed wadding. A spouted cap is provided with the 1 litre presentations.
- 2.5 litre high-density polyethylene flat bottom containers with polypropylene closures and tamper evident with induction heat-sealed wadding. A spouted cap is provided with the 2.5 litre presentations.
- 250 ml high density polyethylene flexipacks with twin neck dispenser, internal graduated calibration chamber and polypropylene heat-sealed screw cap.
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:
- Bimeda Animal Health Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Bimeda Animal Health Limited
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/DCP/16/0001
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0293/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 22/01/2025