OXYTETRAVIT
OXYTETRAVIT
Authorised
- Oxytetracycline hydrochloride
- RETINOL ACETATE
- Colecalciferol
- ALPHATOCOPHEROL ACETATE
- VITAMIN K
- Ascorbic acid
- Thiamine hydrochloride
- Riboflavin
- Pyridoxine hydrochloride
- Cyanocobalamin
- Folic acid
- Pantothenic acid
- Nicotinic acid
- Biotin
Product identification
Medicine name:
OXYTETRAVIT
ОКСИТЕТРАВИТ
Active substance:
- Oxytetracycline hydrochloride
- RETINOL ACETATE
- Colecalciferol
- ALPHATOCOPHEROL ACETATE
- VITAMIN K
- Ascorbic acid
- Thiamine hydrochloride
- Riboflavin
- Pyridoxine hydrochloride
- Cyanocobalamin
- Folic acid
- Pantothenic acid
- Nicotinic acid
- Biotin
Target species:
-
Chicken (hen)
-
Turkey
-
Pig (piglet)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride5.00gram(s)100.00gram(s)
-
RETINOL ACETATE50000.00international unit(s)100.00gram(s)
-
Colecalciferol5000.00international unit(s)100.00gram(s)
-
ALPHATOCOPHEROL ACETATE7.00milligram(s)100.00gram(s)
-
VITAMIN K10.00milligram(s)100.00gram(s)
-
Ascorbic acid250.00milligram(s)100.00gram(s)
-
Thiamine hydrochloride6.60milligram(s)100.00gram(s)
-
Riboflavin25.00milligram(s)100.00gram(s)
-
Pyridoxine hydrochloride10.00milligram(s)100.00gram(s)
-
Cyanocobalamin0.03milligram(s)100.00gram(s)
-
Folic acid1.00milligram(s)100.00gram(s)
-
Pantothenic acid50.00milligram(s)100.00gram(s)
-
Nicotinic acid130.00milligram(s)100.00gram(s)
-
Biotin0.35milligram(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:
- QD06AA53
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:
- Farmavet OOD
Responsible authority:
- Bulgarian Agency For Food Safety
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: 31/08/2022
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: 31/08/2022
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