NEOTYL, unguent intramamar
NEOTYL, unguent intramamar
Authorised
- NEOMYCIN SULFATE
- Prednisolone
- Retinol palmitate
- Tylosin tartrate
Product identification
Medicine name:
NEOTYL, unguent intramamar
Active substance:
- NEOMYCIN SULFATE
- Prednisolone
- Retinol palmitate
- Tylosin tartrate
Target species:
-
Cattle (cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE100.00milligram(s)1.00Syringe
-
Prednisolone10.00milligram(s)1.00Syringe
-
Retinol palmitate10000.00international unit(s)1.00Syringe
-
Tylosin tartrate250.00milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary ointment
Withdrawal period by route of administration:
-
Intramammary use
- Cattle (cow)
-
Meat and offal7day
-
Milk3day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RV01
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Pasteur Filiala Filipesti S.A.
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 150398
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.
Romanian (PDF)
Published on: 20/04/2022
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