MAMIFORT SECADO 250/500 mg SUSPENSIÓN INTRAMAMARIA PARA BOVINO
MAMIFORT SECADO 250/500 mg SUSPENSIÓN INTRAMAMARIA PARA BOVINO
Authorised
- Cloxacillin hemibenzathine
- Ampicillin trihydrate
Product identification
Medicine name:
MAMIFORT SECADO 250/500 mg SUSPENSIÓN INTRAMAMARIA PARA BOVINO
Active substance:
- Cloxacillin hemibenzathine
- Ampicillin trihydrate
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin hemibenzathine500.00milligram(s)1.00Syringe
-
Ampicillin trihydrate250.00milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal28day
-
Milkno withdrawal periodLeche:12 h /50 días + 12 h
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CR50
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Available in:
-
Spain
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:
- Laboratorios Syva S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Syva S.A.
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 914 ESP
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.
Spanish (PDF)
Published on: 29/11/2023
Package Leaflet
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in another language below.
Spanish (PDF)
Published on: 29/11/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 29/11/2023
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