RINGER LATTATO GALENICA SENESE
RINGER LATTATO GALENICA SENESE
Authorised
- Water for injection
- Sodium lactate
- Potassium chloride
- Sodium chloride
- Calcium chloride dihydrate
Product identification
Medicine name:
RINGER LATTATO GALENICA SENESE
Active substance:
- Water for injection
- Sodium lactate
- Potassium chloride
- Sodium chloride
- Calcium chloride dihydrate
Target species:
-
All animal species
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Water for injection1000.00/millilitre(s)1000.00millilitre(s)
-
Sodium lactate3.25/gram(s)1000.00millilitre(s)
-
Potassium chloride0.40/gram(s)1000.00millilitre(s)
-
Sodium chloride6.00/gram(s)1000.00millilitre(s)
-
Calcium chloride dihydrate0.27/gram(s)1000.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
-
All animal species
-
Unspecified0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB05BB01
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
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:
- Industria Farmaceutica Galenica Senese S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
- Industria Farmaceutica Galenica Senese S.r.l.
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet