OXYTETRAVIT
OXYTETRAVIT
Authorised
- Biotin
- Nicotinic acid
- Pantothenic acid
- Folic acid
- Cyanocobalamin
- Pyridoxine hydrochloride
- Riboflavin
- Thiamine hydrochloride
- Ascorbic acid
- VITAMIN K
- ALPHATOCOPHEROL ACETATE
- Colecalciferol
- RETINOL ACETATE
- Oxytetracycline hydrochloride
Product identification
Medicine name:
OXYTETRAVIT
ОКСИТЕТРАВИТ
Active substance:
- Biotin
- Nicotinic acid
- Pantothenic acid
- Folic acid
- Cyanocobalamin
- Pyridoxine hydrochloride
- Riboflavin
- Thiamine hydrochloride
- Ascorbic acid
- VITAMIN K
- ALPHATOCOPHEROL ACETATE
- Colecalciferol
- RETINOL ACETATE
- Oxytetracycline hydrochloride
Target species:
-
Chicken (hen)
-
Turkey
-
Pig (piglet)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Biotin0.35/milligram(s)100.00gram(s)
-
Nicotinic acid130.00/milligram(s)100.00gram(s)
-
Pantothenic acid50.00/milligram(s)100.00gram(s)
-
Folic acid1.00/milligram(s)100.00gram(s)
-
Cyanocobalamin0.03/milligram(s)100.00gram(s)
-
Pyridoxine hydrochloride10.00/milligram(s)100.00gram(s)
-
Riboflavin25.00/milligram(s)100.00gram(s)
-
Thiamine hydrochloride6.60/milligram(s)100.00gram(s)
-
Ascorbic acid250.00/milligram(s)100.00gram(s)
-
VITAMIN K10.00/milligram(s)100.00gram(s)
-
ALPHATOCOPHEROL ACETATE7.00/milligram(s)100.00gram(s)
-
Colecalciferol5000.00/international unit(s)100.00gram(s)
-
RETINOL ACETATE50000.00/international unit(s)100.00gram(s)
-
Oxytetracycline hydrochloride5.00/gram(s)100.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken (hen)
-
Meat and offal7day
-
Egg14day
-
-
Turkey
-
Meat and offal7day
-
Egg14day
-
-
Pig (piglet)
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA56
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Farma Vet OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Farma Vet OOD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2668
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.
Bulgarian (PDF)
Published on: 16/07/2024
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 16/07/2024