NOVACOC FORTE soluție perfuzabilă pentru cai, bovine, porci
NOVACOC FORTE soluție perfuzabilă pentru cai, bovine, porci
Authorised
- Sodium dihydrogen phosphate dihydrate
- Metamizole sodium
- Magnesium gluconate
- Glucose
- Calcium gluconate
- Caffeine
- Acetylmethionine
Product identification
Medicine name:
NOVACOC FORTE soluție perfuzabilă pentru cai, bovine, porci
Active substance:
- Sodium dihydrogen phosphate dihydrate
- Metamizole sodium
- Magnesium gluconate
- Glucose
- Calcium gluconate
- Caffeine
- Acetylmethionine
Target species:
-
Horse
-
Cattle
-
Pig
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Sodium dihydrogen phosphate dihydrate4.02/milligram(s)1.00millilitre(s)
-
Metamizole sodium40.00/milligram(s)1.00millilitre(s)
-
Magnesium gluconate10.00/milligram(s)1.00millilitre(s)
-
Glucose181.82/milligram(s)1.00millilitre(s)
-
Calcium gluconate100.00/milligram(s)1.00millilitre(s)
-
Caffeine3.50/milligram(s)1.00millilitre(s)
-
Acetylmethionine40.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
-
Horse
-
Meat and offal6dayDo not use in milk-producing mares for human consumption.
-
-
Cattle
-
Meat and offal13day
-
Milk3day
-
-
Pig
-
Meat and offal6day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BB52
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Package description:
- Available only in Romanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetviva Richter GmbH
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 230038
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Published on: 24/12/2025