NOROLYTE ΚΟΝΙΣ ΓΙΑ ΠΟΣΙΜΟ ΔΙΑΛΥΜΑ
NOROLYTE ΚΟΝΙΣ ΓΙΑ ΠΟΣΙΜΟ ΔΙΑΛΥΜΑ
Authorised
- Sodium citrate
- Sodium acetate
- Sodium propionate
- Sodium chloride
- Potassium chloride
- Potassium dihydrogen phosphate
- Glucose
Product identification
Medicine name:
NOROLYTE ΚΟΝΙΣ ΓΙΑ ΠΟΣΙΜΟ ΔΙΑΛΥΜΑ
Active substance:
- Sodium citrate
- Sodium acetate
- Sodium propionate
- Sodium chloride
- Potassium chloride
- Potassium dihydrogen phosphate
- Glucose
Target species:
-
Cattle
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Sodium citrate4.68/gram(s)100.00gram(s)
-
Sodium acetate3.92/gram(s)100.00gram(s)
-
Sodium propionate2.29/gram(s)100.00gram(s)
-
Sodium chloride5.59/gram(s)100.00gram(s)
-
Potassium chloride3.56/gram(s)100.00gram(s)
-
Potassium dihydrogen phosphate1.62/gram(s)100.00gram(s)
-
Glucose75.24/gram(s)100.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07CQ
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Chellafarm Vet Α.Ε.
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories (Ireland) Limited
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 5416/K-2646/10-05-1994/K-0094001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet