TETRANEOMAST F
TETRANEOMAST F
Authorised
- Tetracycline hydrochloride
- NEOMYCIN SULFATE
- Prednisolone acetate
Product identification
Medicine name:
ТЕТРАНЕОМАСТ Ф
TETRANEOMAST F
Active substance:
- Tetracycline hydrochloride
- NEOMYCIN SULFATE
- Prednisolone acetate
Target species:
-
Cattle (lactating cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Tetracycline hydrochloride200.00/milligram(s)8.00gram(s)
-
NEOMYCIN SULFATE250.00/milligram(s)8.00gram(s)
-
Prednisolone acetate10.00/milligram(s)8.00gram(s)
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle (lactating cow)
-
Meat and offal14day
-
Milk5day5 дни (10 издоявания)
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RV01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Available only in Bulgarian
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:
- Farma Vet OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Farmavet OOD
Responsible authority:
- Bulgarian Agency For Food Safety
Authorisation number:
- 0022-2760
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: 23/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 23/02/2022
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