Estrumate 250 micrograms/ml solution for injection
Estrumate 250 micrograms/ml solution for injection
Not authorised
- Cloprostenol sodium
Product identification
Medicine name:
Estrumat vet. 0,25 mg/ml stungulyf, lausn, handa nautgripum, svínum og hestum
Estrumate 250 micrograms/ml solution for injection
Active substance:
- Cloprostenol sodium
Target species:
-
Cattle
-
Equid
-
Goat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Cloprostenol sodium0.26/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal1day
-
Milk0day
-
-
Equid
-
Meat and offal1day
-
Milk0day
-
-
Goat
-
Meat and offal1day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG02AD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Iceland
Package description:
- 1 x 10 ml bottle
- 1 x 20 ml bottle
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vet Pharma Friesoythe GmbH
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- 880024
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.
Icelandic (PDF)
Published on: 16/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Icelandic (PDF)
Published on: 16/02/2022
Combined File of all Documents
English (PDF)
Download Published on: 17/12/2025
Icelandic (PDF)
Published on: 13/08/2025