Analeptol 50 mg/ml + 50 mg/ml solution for injection for cattle, horses, pigs, dogs and cats
Analeptol 50 mg/ml + 50 mg/ml solution for injection for cattle, horses, pigs, dogs and cats
Authorised
- Heptaminol
- Diprophylline
Product identification
Medicine name:
Analeptol 50 mg/ml + 50 mg/ml solution for injection for cattle, horses, pigs, dogs and cats
Analeptol 50 mg/ml + 50 mg/ml Injektionslösung für Rinder, Pferde, Schweine, Hunde und Katzen
Active substance:
- Heptaminol
- Diprophylline
Target species:
-
Cattle
-
Horse
-
Pig
-
Cattle (calf)
-
Horse (foal)
-
Pig (piglet)
-
Dog
-
Cat
Route of administration:
-
Intravenous use
-
Intraperitoneal use
-
Intramuscular use
Product details
Active substance and strength:
-
Heptaminol50.00milligram(s)1.00millilitre(s)
-
Diprophylline50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
- Cattle
-
Meat and offal2day
-
Milk48hour
-
- Horse
-
Meat and offal2day
-
Milk48hour
-
- Pig
-
Meat and offal2day
-
- Cattle (calf)
-
Meat and offal2day
-
- Horse (foal)
-
Meat and offal2day
-
- Pig (piglet)
-
Meat and offal2day
-
- Dog
- Cat
-
Intraperitoneal use
- Cattle
-
Meat and offal2day
-
Milk48hour
-
- Horse
-
Meat and offal2day
-
Milk48hour
-
- Pig
-
Meat and offal2day
-
- Cattle (calf)
-
Meat and offal2day
-
- Horse (foal)
-
Meat and offal2day
-
- Pig (piglet)
-
Meat and offal2day
-
- Dog
- Cat
-
Intramuscular use
- Cattle (calf)
-
Meat and offal7day
-
- Horse (foal)
-
Meat and offal7day
-
- Pig (piglet)
-
Meat and offal7day
-
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QR03DA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Available in:
-
Austria
Package description:
- Carton box containing 1 clear type I glass vial containing 50 ml closed with a grey bromobutyl rubber stopper and aluminium cap.
- Carton box containing 1 clear type I glass vial containing 20 ml closed with a grey bromobutyl rubber stopper and aluminium cap.
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:
- CP-Pharma Handelsgesellschaft mbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Cp-Pharma Handelsgesellschaft mbH
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 841644
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0379/001
Concerned member states:
-
Austria
-
Belgium
-
Estonia
-
France
-
Germany
-
Hungary
-
Ireland
-
Italy
-
Portugal
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 28/07/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 24/03/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 24/03/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 24/03/2023
How useful was this page?: