Cylabel 1000 mg/g powder for use in drinking water/milk for cattle and pigs
Cylabel 1000 mg/g powder for use in drinking water/milk for cattle and pigs
Not authorised
- Sodium salicylate
Product identification
Medicine name:
Cylabel 1000 mg/g powder for use in drinking water/milk for cattle and pigs
Cylabel, 1000 mg/g milteliai naudoti su geriamuoju vandeniu ar pienu galvijams ir kiaulėms
Active substance:
- Sodium salicylate
Target species:
-
Cattle (pre-ruminant)
-
Pig
Route of administration:
-
In drinking water use
-
In drinking water/milk use
-
In drinking water/milk use
Product details
Active substance and strength:
-
Sodium salicylate1000.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In drinking water use
- Cattle (pre-ruminant)
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
-
In drinking water/milk use
- Cattle (pre-ruminant)
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
-
In drinking water/milk use
- Cattle (pre-ruminant)
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Lithuania
Package description:
- (ID2): 1 unspecified outer container with 1 Sachet (PolyEthylene, Paper, PolyEthylene, Aluminium, PolyEthylene) with 5 kilogram(s) (5 kilogram(s))
- (ID1): 1 unspecified outer container with 1 Box (Paper, PolyEthylene, Aluminium, PolyEthylene) with 1 kilogram(s) (1 kilogram(s))
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:
- Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- SFVS
Authorisation number:
- LT/2/17/2415/001-002
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0169/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?: