Adrenaline, 1 mg/ml oplossing voor injectie
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Adrenalin
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Valid
Authorised in these countries:
-
Netherlands
Page contents
Product identification
Medicine name:
Adrenaline, 1 mg/ml oplossing voor injectie
Active substance and strength:
-
Adrenalin1.00milligram(s)1.00millilitre(s)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC01CA24
Authorisation number:
- REG NL 4756
Product identification number:
- cdd3248d-5a08-448c-9f1f-3a457753def1
Permanent identification number:
- 600000067598
Product details
Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
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Intramuscular use
- Cattle
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Milk
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Meat and offal
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Meat and offal1day
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Meat and offal1day
-
- Sheep
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Milk
-
Meat and offal1day
-
- Horse
-
Meat and offal
-
Meat and offal1day
-
Meat and offal1day
-
- Pig
-
Meat and offal1day
-
- Dog
-
Intravenous use
- Cattle
-
Milk
-
Meat and offal
-
Meat and offal1day
-
Meat and offal1day
-
- Sheep
-
Milk
-
Meat and offal1day
-
- Horse
-
Meat and offal
-
Meat and offal1day
-
Meat and offal1day
-
- Pig
-
Meat and offal1day
-
- Dog
-
Subcutaneous use
- Cattle
-
Milk
-
Meat and offal
-
Meat and offal1day
-
Meat and offal1day
-
- Sheep
-
Milk
-
Meat and offal1day
-
- Horse
-
Meat and offal
-
Meat and offal1day
-
Meat and offal1day
-
- Pig
-
Meat and offal1day
-
- Dog
Availability
Package description:
- Available only in Nederlands
- Available only in Nederlands
Manufacturing sites for batch release:
- Kela - Kempisch Laboratorium - Kela Laboratoria
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.
Authorisation details
Authorisation status:
-
Valid
Authorisation procedure type:
-
Marketing Authorisation
Procedure number:
This information is not available for this product.
Date of authorisation status change:
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Authorisation country:
-
Netherlands
Responsible authority:
- Medicines Evaluation Board
Marketing authorisation holder:
- Alfasan Nederland B.V.
Marketing authorisation issued:
Reference member state:
This information is not available for this product.
Concerned member states:
This information is not available for this product.
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.
Additional information
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
First published:
Last updated:
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