GAMALC, (166+34+50+220)MG/ML ενέσιμο διάλυμα για πρόβατα
GAMALC, (166+34+50+220)MG/ML ενέσιμο διάλυμα για πρόβατα
Authorised
- Calcium gluconate
- Boric acid
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Lactose monohydrate
Product identification
Medicine name:
GAMALC, (166+34+50+220)MG/ML ενέσιμο διάλυμα για πρόβατα
Active substance:
- Calcium gluconate
- Boric acid
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Lactose monohydrate
Target species:
-
Sheep
Route of administration:
-
Submucosal use
-
Intravenous bolus use
Product details
Active substance and strength:
-
Calcium gluconate166.00milligram(s)1.00millilitre(s)
-
Boric acid34.00milligram(s)1.00millilitre(s)
-
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE50.00milligram(s)1.00millilitre(s)
-
Lactose monohydrate220.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Submucosal use
-
Sheep
-
Meat and offal, milkno withdrawal periodΔεν εφαρμόζεται
-
-
-
Intravenous bolus use
-
Sheep
-
Meat and offal, milkno withdrawal periodΔεν εφαρμόζεται
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Package description:
- Available only in Greek
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Hellafarm S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories (Ireland) Limited
- Norbrook Laboratories (Ireland) Limited
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 27485/24-11-2004/K-0155301
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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