Veterinary Medicines

Cylabel 1000 mg/g powder for use in drinking water/milk for cattle and pigs

Not authorised
  • Sodium salicylate
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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 salicylate
    1000.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • In drinking water use
    • Cattle (pre-ruminant)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • In drinking water/milk use
    • Cattle (pre-ruminant)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • In drinking water/milk use
    • Cattle (pre-ruminant)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
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

Documents

Summary of Product Characteristics

English (PDF)
Published on: 31/08/2022
Download

Combined File of all Documents

English (PDF)
Published on: 31/08/2022
Download

RV2415.pdf

Lithuanian (PDF)
Published on: 30/05/2022
Download
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