Tenazym perorálna suspenzia
Tenazym perorálna suspenzia
Authorised
- Tetracycline hydrochloride
- NEOMYCIN SULFATE
- Prednisolone acetate
- Chymotrypsin
- Trypsin
- Papain
Product identification
Medicine name:
Tenazym perorálna suspenzia
Active substance:
- Tetracycline hydrochloride
- NEOMYCIN SULFATE
- Prednisolone acetate
- Chymotrypsin
- Trypsin
- Papain
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
-
Cutaneous use
Product details
Active substance and strength:
-
Tetracycline hydrochloride30.00milligram(s)1.00millilitre(s)
-
NEOMYCIN SULFATE22.50milligram(s)1.00millilitre(s)
-
Prednisolone acetate2.00milligram(s)1.00millilitre(s)
-
Chymotrypsin120.00FIP1.00millilitre(s)
-
Trypsin12.00FIP1.00millilitre(s)
-
Papain1.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
- Dog
- Cat
-
Cutaneous use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA53
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Veyx Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Veyx Pharma GmbH
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/084/97-S
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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Slovak (PDF)
Published on: 24/01/2022
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