LINKOLAKTAN, 750 mg, intramaminis gelis melžiamoms karvėms
LINKOLAKTAN, 750 mg, intramaminis gelis melžiamoms karvėms
Authorised
- Lincomycin
Product identification
Medicine name:
LINKOLAKTAN, 750 mg, intramaminis gelis melžiamoms karvėms
Active substance:
- Lincomycin
Target species:
-
Cattle (lactating cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Lincomycin750.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary gel
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (lactating cow)
-
Meat and offal3day
-
Milk84hour84 Hours or 7 milkings.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51FF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Available in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/15/2308/001-002
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.
Lithuanian (PDF)
Published on: 15/10/2025
How useful was this page?: