Pederipra Spray 20 mg/ml uz ādas lietojams aerosols, suspensija liellopiem, zirgiem, cūkām, aitām, kazām, suņiem, kaķiem, trušiem un mājputniem
Pederipra Spray 20 mg/ml uz ādas lietojams aerosols, suspensija liellopiem, zirgiem, cūkām, aitām, kazām, suņiem, kaķiem, trušiem un mājputniem
Not authorised
- Chlortetracycline
Product identification
Medicine name:
Pederipra Spray 20 mg/ml uz ādas lietojams aerosols, suspensija liellopiem, zirgiem, cūkām, aitām, kazām, suņiem, kaķiem, trušiem un mājputniem
Active substance:
- Chlortetracycline
Target species:
-
Dog
-
Pig
-
Rabbit
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Poultry
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Horse
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Cattle
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Goat
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Cat
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Sheep
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Chlortetracycline20.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous spray, suspension
Withdrawal period by route of administration:
-
Cutaneous use
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Pig
-
Meat and offal0day
-
-
Rabbit
-
Meat and offal0day
-
-
Poultry
-
Meat and offal0day
-
Eggs0day
-
-
Horse
-
Milk0day
-
Meat and offal0dayNelietot uz tesmeņa dzīvniekiem laktācijas laikā, ja pienu paredzēts lietot cilvēku uzturā.
-
-
Cattle
-
Milk0day
-
Meat and offal0dayNelietot uz tesmeņa dzīvniekiem laktācijas laikā, ja pienu paredzēts lietot cilvēku uzturā.
-
-
Goat
-
Meat and offal0dayNelietot uz tesmeņa dzīvniekiem laktācijas laikā, ja pienu paredzēts lietot cilvēku uzturā.
-
Milk0day
-
-
Sheep
-
Milk0day
-
Meat and offal0dayNelietot uz tesmeņa dzīvniekiem laktācijas laikā, ja pienu paredzēts lietot cilvēku uzturā.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/97/0611
Date of authorisation status change:
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.
Latvian (PDF)
Published on: 24/04/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 24/04/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 24/04/2024