Ultrapen LA, 300 mg/ml, süstesuspensioon veistele ja sigadele
Ultrapen LA, 300 mg/ml, süstesuspensioon veistele ja sigadele
Authorised
- Benzylpenicillin procaine
Product identification
Medicine name:
Ultrapen LA, 300 mg/ml, süstesuspensioon veistele ja sigadele
Active substance:
- Benzylpenicillin procaine
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Benzylpenicillin procaine300.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal21day
-
Milk8daypiim: 8 päeva (192 tundi)
-
- Pig
-
Meat and offal10day
-
-
Subcutaneous use
- Cattle
-
Meat and offal13day
-
Milkno withdrawal periodSubkutaanseks kasutamiseks mittelakteerivatel veistel
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CE09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Manufacturing Limited
- Norbrook Laboratories Limited
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1227
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.
Estonian (PDF)
Published on: 24/01/2022
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