Neofort 700 mg/g Proszek do sporządzania roztworu doustnego
Neofort 700 mg/g Proszek do sporządzania roztworu doustnego
Authorised
- NEOMYCIN SULFATE
Product identification
Medicine name:
Neofort 700 mg/g Proszek do sporządzania roztworu doustnego
Active substance:
- NEOMYCIN SULFATE
Target species:
-
Turkey
-
Pig
-
Sheep
-
Cattle
-
Chicken (hen)
-
Goat
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE700.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
In drinking water/milk use
- Turkey
-
Meat and offal7day
-
- Pig
-
Meat and offal14day
-
- Sheep
-
Meat and offal14day
-
- Cattle
-
Meat and offal14day
-
- Chicken (hen)
-
Meat and offal7day
-
- Goat
-
Meat and offal14day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Available in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Biofaktor Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Biofaktor Sp. z o.o.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0425
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 16/03/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 16/03/2022
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