MASTICEN SECADO, intramaminė suspensija
MASTICEN SECADO, intramaminė suspensija
Authorised
- Cloxacillin hemibenzathine
Product identification
Medicine name:
MASTICEN SECADO, intramaminė suspensija
Active substance:
- Cloxacillin hemibenzathine
Target species:
-
Cattle (cow)
-
Sheep
-
Goat
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin hemibenzathine1000.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (cow)
-
Meat and offal0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Sheep
-
Meat and offal0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Goat
-
Meat and offal0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised 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:
- Vetmarket UAB
Marketing authorisation date:
Manufacturing sites for batch release:
- Cenavisa S.L.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/02/1410/001-002
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
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in another language below.
Lithuanian (PDF)
Published on: 23/12/2025
