Veterinary Medicines

Effydral Tablets

Not authorised
  • Glycine
  • Citric acid
  • Lactose monohydrate
  • Potassium chloride
  • Sodium chloride
  • Sodium hydrogen carbonate
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Product identification

Medicine name:
Effydral Tablets
Active substance:
  • Glycine
  • Citric acid
  • Lactose monohydrate
  • Potassium chloride
  • Sodium chloride
  • Sodium hydrogen carbonate
Target species:
  • Cattle
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Glycine
    2.25
    gram(s)
    /
    1.00
    Tablet
  • Citric acid
    3.84
    gram(s)
    /
    1.00
    Tablet
  • Lactose monohydrate
    32.44
    gram(s)
    /
    1.00
    Tablet
  • Potassium chloride
    1.12
    gram(s)
    /
    1.00
    Tablet
  • Sodium chloride
    2.34
    gram(s)
    /
    1.00
    Tablet
  • Sodium hydrogen carbonate
    6.72
    gram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Effervescent tablet
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05XA
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Ireland
Package description:
  • Aluminium tubs covered with aluminium foil containing a round, white, effervescent tablet with flat end surfaces and bevelled edges.�The diameter is about 52 mm and the height is about 19 mm.�The mean tablet weight is about 48.7 g.�One cardboard box contains 48 tablets packed in inner cartons of 6 x 8 tablets.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Zoetis Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Aurovitas Nederland B.V.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10387/024/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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