UNOFLOX 100 mg/ml solution for injection.
UNOFLOX 100 mg/ml solution for injection.
Not authorised
- Enrofloxacin
Product identification
Medicine name:
UNOFLOX 100 mg/ml solution for injection.
Unoflox 100 mg / ml solução injetável
Active substance:
- Enrofloxacin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offalno withdrawal periodMeat and offal: s.c.: 14 days/i.v.: 7 days
-
Milkno withdrawal periodMilk: sc: 120 houras (5 days)/i.v 72 hours (3 days)
-
- Pig
-
Meat and offal12day
-
-
Subcutaneous use
- Cattle
-
Meat and offalno withdrawal periodMeat and offal: s.c.: 14 days/i.v.: 7 days
-
Milkno withdrawal periodMilk: sc: 120 houras (5 days)/i.v 72 hours (3 days)
-
- Pig
-
Meat and offal12day
-
-
Intravenous use
- Cattle
-
Meat and offalno withdrawal periodMeat and offal: s.c.: 14 days/i.v.: 7 days
-
Milkno withdrawal periodMilk: sc: 120 houras (5 days)/i.v 72 hours (3 days)
-
- Pig
-
Meat and offal12day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Revoked
Authorised in:
-
Portugal
Package description:
- box containing 10 polypropylene vials of 250 ml
- box containing 10 polypropylene vials of 100 ml
- box containing 1 polypropylene vial of 250 ml
- box containing 1 polypropylene vial of 100 ml
- box 10 glass vials of 250 ml
- box containing 10 glass vials of 100 ml
- box containing 1 glass vial of 250 ml
- box containing 1 glass vial of 100 ml
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:
- S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 1249/01/19DFVPT
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0299/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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