Cepravin Dry Cow 250 mg Intramammary suspension
Cepravin Dry Cow 250 mg Intramammary suspension
Not authorised
- Cefalonium dihydrate
Product identification
Medicine name:
Cepravin Dry Cow 250 mg, intramammaarsuspensioon
Cepravin Dry Cow 250 mg Intramammary suspension
Active substance:
- Cefalonium dihydrate
Target species:
-
Cattle (dairy cow at drying-off)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cefalonium dihydrate269.60milligram(s)3.00gram(s)
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dairy cow at drying-off)
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51DB90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Estonia
Package description:
- (ID2) 432 gram(s): Behältnis with 144 Syringe (PolyEthylene) each with 3 gram(s), closed with Lid (PolyEthylene)
- (ID1) 60 gram(s): Box (Cardboard) with 20 Syringe (PolyEthylene) each with 3 gram(s), closed with Lid (PolyEthylene)
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Trirx Segre
- Intervet International GmbH
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1729
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0184/001
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.
Estonian (PDF)
Published on: 4/04/2023
Combined File of all Documents
English (PDF)
Download Published on: 30/01/2024
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