CALCIUM BIOTIKA 50 % w/v injekčný roztok
CALCIUM BIOTIKA 50 % w/v injekčný roztok
Not authorised
- Calcium gluconate monohydrate
- Calcium carbonate
- Calcium saccharate
Product identification
Medicine name:
CALCIUM BIOTIKA 50 % w/v injekčný roztok
Active substance:
- Calcium gluconate monohydrate
- Calcium carbonate
- Calcium saccharate
Target species:
-
Cattle
-
Horse
-
Pig
-
Sheep
-
Goat
-
Dog
Route of administration:
-
Intravenous use
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Calcium gluconate monohydrate350.00/milligram(s)1.00millilitre(s)
-
Calcium carbonate27.30/milligram(s)1.00millilitre(s)
-
Calcium saccharate20.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
All relevant tissues0dayZero days
-
-
Horse
-
All relevant tissues0dayZero days
-
-
Pig
-
All relevant tissues0dayZero days
-
-
Sheep
-
All relevant tissues0dayZero days
-
-
Goat
-
All relevant tissues0dayZero days
-
-
-
Intramuscular use
-
Cattle
-
All relevant tissuesno withdrawal periodZero days
-
-
Horse
-
All relevant tissuesno withdrawal periodZero days
-
-
Pig
-
All relevant tissuesno withdrawal periodZero days
-
-
Sheep
-
All relevant tissuesno withdrawal periodZero days
-
-
Goat
-
All relevant tissuesno withdrawal periodZero days
-
-
-
Subcutaneous use
-
Cattle
-
All relevant tissuesno withdrawal periodZero days
-
-
Horse
-
All relevant tissuesno withdrawal periodZero days
-
-
Pig
-
All relevant tissuesno withdrawal periodZero days
-
-
Sheep
-
All relevant tissuesno withdrawal periodZero days
-
-
Goat
-
All relevant tissuesno withdrawal periodZero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AA20
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- BB Pharma a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Farmacia Martin a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/0262/97-S
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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Slovak (PDF)
Published on: 24/11/2021