Parofor 175 mg/ml Solution for injection
Parofor 175 mg/ml Solution for injection
Authorised
- Paromomycin sulfate
Product identification
Medicine name:
Parofor 175 mg/ml Solution for injection
Parofor 70.000 IU/g poeder voor gebruik in drinkwater, melk of kunstmelk voor niet-herkauwende runderen en varkens
Active substance:
- Paromomycin sulfate
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Paromomycin sulfate250.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal20day20 days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- Parofor 175 mg/ml inj. sol. i.m. vial 100 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet J.S.C.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 113511
Date of authorisation status change:
Reference member state:
-
Belgium
Procedure number:
- BE/V/0027/003
Concerned member states:
-
Czechia
-
Denmark
-
Estonia
-
France
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
Generic of:
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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Dutch (PDF)
Published on: 4/04/2022
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