Veterinary Medicines

Novacoc Forte, otopina za infuziju, konj, govedo i svinja

Authorised
  • Metamizole sodium
  • Caffeine
  • CALCIUM GLUCONATE FOR INJECTION
  • Magnesium gluconate
  • SODIUM DIHYDROGEN PHOSPHATE DIHYDRATE PH. EUR.
  • Acetylmethionine
  • Glucose monohydrate
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Product identification

Medicine name:
Novacoc Forte, otopina za infuziju, konj, govedo i svinja
Active substance:
  • Metamizole sodium
  • Caffeine
  • CALCIUM GLUCONATE FOR INJECTION
  • Magnesium gluconate
  • SODIUM DIHYDROGEN PHOSPHATE DIHYDRATE PH. EUR.
  • Acetylmethionine
  • Glucose monohydrate
Target species:
  • Horse
  • Cattle
  • Pig
Route of administration:
  • Intravenous use

Product details

Active substance and strength:
  • Metamizole sodium
    4.00
    gram(s)
    /
    100.00
    millilitre(s)
  • Caffeine
    0.35
    gram(s)
    /
    100.00
    millilitre(s)
  • CALCIUM GLUCONATE FOR INJECTION
    10.00
    gram(s)
    /
    100.00
    millilitre(s)
  • Magnesium gluconate
    1.00
    gram(s)
    /
    100.00
    millilitre(s)
  • SODIUM DIHYDROGEN PHOSPHATE DIHYDRATE PH. EUR.
    0.40
    gram(s)
    /
    100.00
    millilitre(s)
  • Acetylmethionine
    4.00
    gram(s)
    /
    100.00
    millilitre(s)
  • Glucose monohydrate
    18.18
    gram(s)
    /
    100.00
    millilitre(s)
Pharmaceutical form:
  • Solution for infusion
Withdrawal period by route of administration:
  • Intravenous use
    • Horse
      • Meat and offal
        6
        day
    • Cattle
      • Meat and offal
        13
        day
      • Milk
        60
        hour
    • 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:
  • Croatia
Available in:
  • Croatia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetviva Richter GmbH
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/20-01/225
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Croatian (PDF)
Published on: 21/03/2023
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