Neopen 200000 IU/ml - 100 mg/ml Suspensie voor injectie
Neopen 200000 IU/ml - 100 mg/ml Suspensie voor injectie
Authorised
- Benzylpenicillin procaine
- NEOMYCIN SULFATE
Product identification
Medicine name:
Neopen 200000 IU/ml - 100 mg/ml Suspensie voor injectie
Neopen 200000 IU/ml - 100 mg/ml Suspension injectable
Neopen 200000 IU/ml - 100 mg/ml Injektionssuspension
Active substance:
- Benzylpenicillin procaine
- NEOMYCIN SULFATE
Target species:
-
Sheep
-
Cat
-
Pig
-
Dog
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Benzylpenicillin procaine200000.00/international unit(s)1.00millilitre(s)
-
NEOMYCIN SULFATE144.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal56day
-
-
Pig
-
Meat and offal45day
-
-
Cattle
-
Meat and offal89day
-
Milk4day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal89day
-
Meat and offal4day
-
-
Sheep
-
Meat and offal56day
-
-
Pig
-
Meat and offal45day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Neopen 250 ml glass Bottle Suspension for injection
- Neopen 100 ml glass Bottle Suspension for injection
- Neopen 250 ml PET Bottle Suspension for injection
- Neopen 100 ml PET Bottle Suspension for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Productions S.r.l.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
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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Package Leaflet
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Labelling
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