Poviderm Sol 30 mg/g Oplossing voor cutaan gebruik
Poviderm Sol 30 mg/g Oplossing voor cutaan gebruik
Authorised
- POVIDONE, IODINATED
Product identification
Medicine name:
Poviderm Sol 30 mg/g Oplossing voor cutaan gebruik
Poviderm Sol 30 mg/g Solution pour application cutanée
Poviderm Sol 30 mg/g Lösung zur Anwendung auf der Haut
Active substance:
- POVIDONE, IODINATED
Target species:
-
Rabbit
-
Dog
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
POVIDONE, IODINATED30.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Cutaneous solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Rabbit
-
All relevant tissuesno withdrawal periodNot applicable
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD08AG02
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Poviderm Sol 24 Bottles with 4600 g Cutaneous solution
- Poviderm Sol 24 Bottles with 2300 g Cutaneous solution
- Poviderm Sol 24 Bottles with 1840 g Cutaneous solution
- Poviderm Sol 24 Bottles with 920 g Cutaneous solution
- Poviderm Sol 24 Bottles with 460 g Cutaneous solution
- Poviderm Sol 24 Bottles with 230 g Cutaneous solution
- Poviderm Sol 20 Bottles with 4600 g Cutaneous solution
- Poviderm Sol 20 Bottles with 2300 g Cutaneous solution
- Poviderm Sol 20 Bottles with 1840 g Cutaneous solution
- Poviderm Sol 20 Bottles with 920 g Cutaneous solution
- Poviderm Sol 20 Bottles with 460 g Cutaneous solution
- Poviderm Sol 20 Bottles with 230 g Cutaneous solution
- Poviderm Sol 16 Bottles with 4600 g Cutaneous solution
- Poviderm Sol 16 Bottles with 2300 g Cutaneous solution
- Poviderm Sol 16 Bottles with 1840 g Cutaneous solution
- Poviderm Sol 16 Bottles with 920 g Cutaneous solution
- Poviderm Sol 16 Bottles with 460 g Cutaneous solution
- Poviderm Sol 16 Bottles with 230 g Cutaneous solution
- Poviderm Sol 12 4600 g Bottle Cutaneous solution
- Poviderm Sol 12 2300 g Bottle Cutaneous solution
- Poviderm Sol 12 1840 g Bottle Cutaneous solution
- Poviderm Sol 12 920 g Bottle Cutaneous solution
- Poviderm Sol 12 460 g Bottle Cutaneous solution
- Poviderm Sol 12 230 g Bottle Cutaneous solution
- Poviderm Sol 10 4600 g Bottle Cutaneous solution
- Poviderm Sol 10 2300 g Bottle Cutaneous solution
- Poviderm Sol 10 1840 g Bottle Cutaneous solution
- Poviderm Sol 10 920 g Bottle Cutaneous solution
- Poviderm Sol 10 460 g Bottle Cutaneous solution
- Poviderm Sol 10 230 g Bottle Cutaneous solution
- Poviderm Sol 8 4600 g Bottle Cutaneous solution
- Poviderm Sol 8 2300 g Bottle Cutaneous solution
- Poviderm Sol 8 1840 g Bottle Cutaneous solution
- Poviderm Sol 8 920 g Bottle Cutaneous solution
- Poviderm Sol 8 460 g Bottle Cutaneous solution
- Poviderm Sol 8 230 g Bottle Cutaneous solution
- Poviderm Sol 6 4600 g Bottle Cutaneous solution
- Poviderm Sol 6 2300 g Bottle Cutaneous solution
- Poviderm Sol 6 1840 g Bottle Cutaneous solution
- Poviderm Sol 6 920 g Bottle Cutaneous solution
- Poviderm Sol 6 460 g Bottle Cutaneous solution
- Poviderm Sol 6 230 g Bottle Cutaneous solution
- Poviderm Sol 4 4600 g Bottle Cutaneous solution
- Poviderm Sol 4 2300 g Bottle Cutaneous solution
- Poviderm Sol 4 1840 g Bottle Cutaneous solution
- Poviderm Sol 4 920 g Bottle Cutaneous solution
- Poviderm Sol 4 460 g Bottle Cutaneous solution
- Poviderm Sol 4 230 g Bottle Cutaneous solution
- Poviderm Sol 4600 g Bottle Cutaneous solution
- Poviderm Sol 2300 g Bottle Cutaneous solution
- Poviderm Sol 1840 g Bottle Cutaneous solution
- Poviderm Sol 920 g Bottle Cutaneous solution
- Poviderm Sol 460 g Bottle Cutaneous solution
- Poviderm Sol 230 g Bottle Cutaneous solution
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:
- Emdoka
Marketing authorisation date:
Manufacturing sites for batch release:
- Feramed B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V196971
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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Package Leaflet
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Labelling
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