Injectio Glucosi Isotonica et Natrii Chlorati Isotonica 1:1 WET Baxter (25 g + 4,5 g)/1000 ml Roztwór do infuzji
Injectio Glucosi Isotonica et Natrii Chlorati Isotonica 1:1 WET Baxter (25 g + 4,5 g)/1000 ml Roztwór do infuzji
Authorised
- Glucose
- Sodium chloride
Product identification
Medicine name:
Injectio Glucosi Isotonica et Natrii Chlorati Isotonica 1:1 WET Baxter (25 g + 4,5 g)/1000 ml Roztwór do infuzji
Active substance:
- Glucose
- Sodium chloride
Target species:
-
Cattle
-
Goat
-
Cat
-
Dog
-
Pig
-
Horse
-
Sheep
Route of administration:
-
Intraperitoneal use
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Glucose25.00gram(s)1000.00millilitre(s)
-
Sodium chloride4.50gram(s)1000.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intraperitoneal use
- Cattle
-
Meat and offal5week
-
- Goat
-
Meat and offal5week
-
- Cat
- Dog
- Pig
-
Meat and offal5week
-
- Horse
-
Meat and offal5week
-
- Sheep
-
Meat and offal5week
-
-
Subcutaneous use
- Cattle
-
Meat and offal5week
-
- Goat
-
Meat and offal5week
-
- Cat
- Dog
- Pig
-
Meat and offal5week
-
- Horse
-
Meat and offal5week
-
- Sheep
-
Meat and offal5week
-
-
Intravenous use
- Cattle
-
Meat and offal5week
-
- Goat
-
Meat and offal5week
-
- Cat
- Dog
- Pig
-
Meat and offal5week
-
- Horse
-
Meat and offal5week
-
- Sheep
-
Meat and offal5week
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB05BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Baxter Polska Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bieffe Medital S.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0275
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
How useful was this page?: