Beviplex vet. injektioneste, liuos
Beviplex vet. injektioneste, liuos
Authorised
- Cyanocobalamin
- Dexpanthenol
- Nicotinamide
- Pyridoxine hydrochloride
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
Product identification
Medicine name:
Beviplex vet. injektioneste, liuos
Active substance:
- Cyanocobalamin
- Dexpanthenol
- Nicotinamide
- Pyridoxine hydrochloride
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
Target species:
-
Pig
-
Cattle
-
Horse
-
Sheep
-
Dog
-
Mink
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Cyanocobalamin5.00/microgram(s)1.00millilitre(s)
-
Dexpanthenol5.00/milligram(s)1.00millilitre(s)
-
Nicotinamide25.00/milligram(s)1.00millilitre(s)
-
Pyridoxine hydrochloride2.00/milligram(s)1.00millilitre(s)
-
RIBOFLAVIN SODIUM PHOSPHATE3.00/milligram(s)1.00millilitre(s)
-
Thiamine hydrochloride4.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
-
Intravenous use
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11EA
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Finland
Available in:
-
Finland
Package description:
- Available only in Finnish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Pharmaxim AB
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- Finnish Medicines Agency
Authorisation number:
- 7639
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.
Finnish (PDF)
Published on: 3/01/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Finnish (PDF)
Published on: 14/11/2023