Veterinary Medicines

Novacoc forte - Infusionslösung für Tiere

Authorised
  • Glucose monohydrate
  • Metamizole sodium
  • Caffeine
  • Calcium gluconate monohydrate
  • Magnesium gluconate
  • Sodium dihydrogen phosphate dihydrate
  • Acetylmethionine
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Product identification

Medicine name:
Novacoc forte - Infusionslösung für Tiere
Active substance:
  • Glucose monohydrate
  • Metamizole sodium
  • Caffeine
  • Calcium gluconate monohydrate
  • Magnesium gluconate
  • Sodium dihydrogen phosphate dihydrate
  • Acetylmethionine
Target species:
  • Cattle
  • Horse
  • Pig
Route of administration:
  • Intravenous use

Product details

Active substance and strength:
  • Glucose monohydrate
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Metamizole sodium
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Caffeine
    3.50
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium gluconate monohydrate
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium gluconate
    10.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium dihydrogen phosphate dihydrate
    4.02
    milligram(s)
    /
    1.00
    millilitre(s)
  • Acetylmethionine
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for infusion
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        13
        day
      • Milk
        60
        hour
    • Horse
      • Meat and offal
        6
        day
    • Pig
      • Meat and offal
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02BB52
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetviva Richter GmbH
  • Richter Pharma AG
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-00520
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 24/05/2023
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 6/04/2023
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 6/04/2023
Download
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