Kefamast Dry Cow suspensija ievadīšanai tesmenī govīm
Kefamast Dry Cow suspensija ievadīšanai tesmenī govīm
Not authorised
- Cefalexin
- Dihydrostreptomycin
Product identification
Medicine name:
Kefamast Dry Cow suspensija ievadīšanai tesmenī govīm
Active substance:
- Cefalexin
- Dihydrostreptomycin
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cefalexin500.00/milligram(s)1.00Syringe
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Dihydrostreptomycin500.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal28day
-
Milk3dayJa 40 dienu laikā pēc zāļu lietošanas govs dzemdē, pienu pārtikā nedrīkst lietot ātrāk nekā 42,5 dienas pēc zāļu lietošanas.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RD01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Latvia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Bimeda Animal Health Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Bimeda Animal Health Limited
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/95/0348
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
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in another language below.
Latvian (PDF)
Published on: 28/01/2025
Package Leaflet
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in another language below.
Latvian (PDF)
Published on: 28/01/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 28/01/2025