INTRAMAR DRY COW, 600mg, Intramammary suspension
INTRAMAR DRY COW, 600mg, Intramammary suspension
Authorised
- Cloxacillin hemibenzathine
Product identification
Medicine name:
INTRAMAR DRY COW, 600mg, Intramammary suspension
Active substance:
- Cloxacillin hemibenzathine
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin hemibenzathine765.42/milligram(s)1.00Applicator
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal28day
-
Milk96hourafter calving if the dry period is 42 days or longer.
42 days plus 96 hours after treatment in cows with a dry period shorter than 42 days.
The product must not be used in lactating cows.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Plastic Applicator 24 x 1.0 Applicator
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application – bioavailability studies cannot be used to demonstrate bioequivalence (Article 19(1)(b) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-3384
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0216/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
France
-
Ireland
-
Latvia
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Portugal
-
Romania
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
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.
Bulgarian (PDF)
Published on: 5/10/2026
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 5/10/2026
Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 5/10/2026