Ampi-Dry Poeder voor oplossing voor injectie
Ampi-Dry Poeder voor oplossing voor injectie
Authorised
- Ampicillin sodium
Product identification
Medicine name:
Ampi-Dry Poeder voor oplossing voor injectie
Ampi-Dry Poudre pour solution injectable
Ampi-Dry Pulver zur Herstellung einer Injektionslösung
Active substance:
- Ampicillin sodium
Target species:
-
Horse
-
Cattle
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Ampicillin sodium1.00/gram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Horse
-
Meat and offal4day
-
-
Cattle
-
Meat and offal3day
-
Milk48hour4 milkings
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Ampi-Dry 5 g Vial Powder for solution for injection
- Ampi-Dry 3 g Vial Powder for solution 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:
- Prodivet Pharmaceuticals
Marketing authorisation date:
Manufacturing sites for batch release:
- Prodivet Pharmaceuticals
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V104097
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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