CEVAMEC 1 %, injekcinis tirpalas
CEVAMEC 1 %, injekcinis tirpalas
Not authorised
- Ivermectin
Product identification
Medicine name:
CEVAMEC 1 %, injekcinis tirpalas
Active substance:
- Ivermectin
Target species:
-
Cattle
-
Sheep
-
Goat
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal49day
-
Milkno withdrawal periodNot authorized for use in lactating females, whose milk will be used for human consumption and pregnant females, whose milk will be used for human consumption, 28 days before delivery.
-
-
Sheep
-
Meat and offal21day
-
Milkno withdrawal periodNot authorized for use in lactating females, whose milk will be used for human consumption and pregnant females, whose milk will be used for human consumption, 28 days before delivery.
-
-
Goat
-
Meat and offal28day
-
Milkno withdrawal periodNot authorized for use in lactating females, whose milk will be used for human consumption and pregnant females, whose milk will be used for human consumption, 28 days before delivery.
-
-
Pig
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Surrendered
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- CEVA-Phylaxia Zrt.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/00/1080/001-005
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV1080.pdf
Lithuanian (PDF)
Download Published on: 11/08/2022
