REMOPHAN 75 µg/ml injekčný roztok
REMOPHAN 75 µg/ml injekčný roztok
Authorised
- Cloprostenol sodium
Product identification
Medicine name:
REMOPHAN 75 µg/ml injekčný roztok
Active substance:
- Cloprostenol sodium
Target species:
-
Cattle (heifer)
-
Cattle (cow)
-
Pig (sow)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Cloprostenol sodium79.00microgram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle (heifer)
-
Meat and offal24hour
-
-
Cattle (cow)
-
Meat and offal24hour
-
Milk4hour
-
-
Pig (sow)
-
Meat and offal24hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG02AD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 99/104/89-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Slovak (PDF)
Published on: 11/11/2021
How useful was this page?: