TETRA-DELTA 100/105/100/100/10 mg, intramamarna suspenzija, za krave u laktaciji
TETRA-DELTA 100/105/100/100/10 mg, intramamarna suspenzija, za krave u laktaciji
Not authorised
- Prednisolone
- Dihydrostreptomycin
- Benzylpenicillin procaine
- Neomycin
- Novobiocin
Product identification
Medicine name:
TETRA-DELTA 100/105/100/100/10 mg, intramamarna suspenzija, za krave u laktaciji
Active substance:
- Prednisolone
- Dihydrostreptomycin
- Benzylpenicillin procaine
- Neomycin
- Novobiocin
Target species:
-
Cattle (lactating cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Prednisolone10.00/milligram(s)1.00Syringe
-
Dihydrostreptomycin100.00/milligram(s)1.00Syringe
-
Benzylpenicillin procaine100.00/milligram(s)1.00Syringe
-
Neomycin105.00/milligram(s)1.00Syringe
-
Novobiocin100.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (lactating cow)
-
Meat and offal7day
-
Milk108hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RV01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Revoked
Authorised in:
-
Croatia
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:
- Zoetis B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Zoetis Belgium
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/20-01/751
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
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Croatian (PDF)
Published on: 20/02/2022
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