Oxytetraciclin hydrochloride-NGP 7/ 0,340 g, 11/ 0,510 g, 22/ 1,020 g comprettae spumescentes
Oxytetraciclin hydrochloride-NGP 7/ 0,340 g, 11/ 0,510 g, 22/ 1,020 g comprettae spumescentes
Authorised
- Oxytetracycline hydrochloride
- Oxytetracycline hydrochloride
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Окситетрациклин хидрохлорид-NGP 7/ 0,340 g, 11/ 0,510 g, 22/ 1,020 g пенообразуващи компрети
Oxytetraciclin hydrochloride-NGP 7/ 0,340 g, 11/ 0,510 g, 22/ 1,020 g comprettae spumescentes
Active substance:
- Oxytetracycline hydrochloride
- Oxytetracycline hydrochloride
- Oxytetracycline hydrochloride
Target species:
-
Pig (sow for reproduction)
-
Goat
-
Sheep
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride0.34gram(s)1.00Tablet
-
Oxytetracycline hydrochloride0.51gram(s)1.00Tablet
-
Oxytetracycline hydrochloride1.02gram(s)1.00Tablet
Pharmaceutical form:
-
Intrauterine tablet
Withdrawal period by route of administration:
-
Intrauterine use
-
Pig (sow for reproduction)
-
Meat and offalno withdrawal periodМесо и вътрешни органи - третираните животни не може да се използват за консумация от хора
-
-
Goat
-
Milkno withdrawal periodМляко - по време на третирането и най-малко 4-5 дни след това животните отделят коластра, която не се консумира от хора
-
Meat and offalno withdrawal periodМесо и вътрешни органи - третираните животни не може да се използват за консумация от хора
-
-
Sheep
-
Meat and offalno withdrawal periodМесо и вътрешни органи - третираните животни не може да се използват за консумация от хора
-
Milkno withdrawal periodМляко - по време на третирането и най-малко 4-5 дни след това животните отделят коластра, която не се консумира от хора
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA
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:
- Northern Veterinary Dealer-SVD OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Northern Veterinary Dealer-SVD OOD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-1649-03-11-2011
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: 27/03/2025
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: 27/03/2025
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