Veterinary Medicine Information website

DOPHACYL AVI 1000 MG/G POWDER FOR USE IN DRINKING WATER FOR CHICKENS

Authorised
  • Sodium salicylate
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Product identification

Medicine name:
DOPHACYL AVI 1000 MG/G POWDER FOR USE IN DRINKING WATER FOR CHICKENS
Active substance:
  • Sodium salicylate
Target species:
  • Chicken
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Sodium salicylate
    1000.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • Oral use
    • Chicken
      • Meat and offal
        2
        day
      • Eggs
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02BA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Lithuania
Available in:
  • Lithuania
Package description:
  • Bucket: white polypropylene square container provided with a polypropylene lid. The bucket contains 1 kg of product.
  • Bucket: white polypropylene square container provided with a polypropylene lid.The bucket contains 2.5 kg of product.
  • Bucket: white polypropylene square container provided with a polypropylene lid. The bucket contains 5 kg of product.
  • Securitainer: white cylindrical polypropylene container, covered with a low-density polyethylene lid. The securitainer contains 500 g of product.
  • Securitainer: white cylindrical polypropylene container, covered with a low-density polyethylene lid. The securitainer contains 1 kg of product.
  • Sachet: white, heat sealed, 4-layer sachet with a PE inner layer which contains 100 g of product.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application - change in active substance(s) (Article 19(1)(a) of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dopharma B.V.
  • Dopharma France
Responsible authority:
  • State Food And Veterinary Service
Authorisation number:
  • LT/2/24/2840/001-006
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0486/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain

Documents

Combined File of all Documents

English (PDF)
Published on: 27/04/2026
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Lithuanian (PDF)
Published on: 29/10/2025
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eu-puar-frv0486001-mr-rpe1021-en.pdf

English (PDF)
Published on: 8/05/2026
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