FATROXIMIN D.C. 100 mg/5 ml intramamálna masť
FATROXIMIN D.C. 100 mg/5 ml intramamálna masť
Authorised
- Rifaximin
Product identification
Medicine name:
FATROXIMIN D.C. 100 mg/5 ml intramamálna masť
Active substance:
- Rifaximin
Target species:
-
Cattle (dry cow)
-
Buffalo (female)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Rifaximin100.00milligram(s)1.00Applicator
Pharmaceutical form:
-
Intramammary ointment
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal0dayMeat and offal: without withdrawal period, The udder must be excluded from human consumption.
-
Milk0dayMilk: 0 days after calving if the length of dry standing is equal to or longer than 35 days. 35 days after administration if the duration of dry standing is less than 35 days.
-
-
Buffalo (female)
-
Meat and offal0dayMeat and offal: without withdrawal period, The udder must be excluded from human consumption.
-
Milk0dayMilk: 0 days after calving if the length of dry standing is equal to or longer than 35 days. 35 days after administration if the duration of dry standing is less than 35 days.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51XX01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/0638/97-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Published on: 14/12/2021
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