Mastijet Forte suspensija ievadīšanai tesmenī laktējošām govīm
Mastijet Forte suspensija ievadīšanai tesmenī laktējošām govīm
Authorised
- Chlortetracycline hydrochloride
- Neomycin
- Bacitracin
- Prednisolone
Product identification
Medicine name:
Mastijet Forte suspensija ievadīšanai tesmenī laktējošām govīm
Active substance:
- Chlortetracycline hydrochloride
- Neomycin
- Bacitracin
- Prednisolone
Target species:
-
Cattle (lactating cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Chlortetracycline hydrochloride200.00/milligram(s)1.00Syringe
-
Neomycin250.00/milligram(s)1.00Syringe
-
Bacitracin2000.00/international unit(s)1.00Syringe
-
Prednisolone10.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (lactating cow)
-
Meat and offal14day
-
Milk96hourPienam: 96 stundas (8 slaukšanas reizes).
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RV01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/96/0344
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 6/09/2024