ALGENAMIC 40 mg/ml solution for injection
ALGENAMIC 40 mg/ml solution for injection
Authorised
- Tolfenamic acid
Product identification
Medicine name:
ALGENAMIC 40 mg/ml solution for injection
Algenamic 40 mg/ml Oplossing voor injectie
Algenamic 40 mg/ml Solution injectable
Algenamic 40 mg/ml Injektionslösung
Active substance:
- Tolfenamic acid
Target species:
-
Cattle
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Tolfenamic acid40.00milligram(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: 12 days intramuscular use / 4 days intravenous use
-
- Pig
-
Meat and offal16day
-
- Dog
- Cattle
-
Milkno withdrawal periodMilk: Zero days intramuscular use/ 24 hours intravenous use
-
-
Intravenous use
- Cattle
-
Meat and offalno withdrawal periodMeat and offal: 12 days intramuscular use / 4 days intravenous use
-
- Cattle
-
Milkno withdrawal periodMilk: Zero days intramuscular use/ 24 hours intravenous use
-
-
Subcutaneous use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Cardboard box with 15 glass vials of 250 ml
- Cardboard box with 10 glass vials of 100 ml
- Cardboard box with 5 glass vial of 20 ml
- Cardboard box with 1 glass vial of 250 ml
- Cardboard box with 1 glass vial of 100 ml
- Cardboard box with 1 glass vial of 20 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:
- Vetpharma Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Mevet S.A.U.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V591777
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0382/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Cyprus
-
France
-
Germany
-
Greece
-
Italy
-
Poland
-
Portugal
-
Romania
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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