NARCOSTART
NARCOSTART
Authorised
- Dexmedetomidine hydrochloride
Product identification
Medicine name:
NARCOSTART
Active substance:
- Dexmedetomidine hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intravenous use
-
Intramuscular use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Dexmedetomidine hydrochloride1.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
- Dog
-
Intramuscular use
- Dog
-
Subcutaneous use
- Dog
- Cat
-
Intramuscular use
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM91
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Maravet S.R.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Produlab Pharma B.V.
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 200099
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
This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 18/11/2021
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