PRIMOX 500 mg/g, pó para solução oral para vitelos, cordeiros, cabritos, suínos, coelhos e aves de capoeira
PRIMOX 500 mg/g, pó para solução oral para vitelos, cordeiros, cabritos, suínos, coelhos e aves de capoeira
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
PRIMOX 500 mg/g, pó para solução oral para vitelos, cordeiros, cabritos, suínos, coelhos e aves de capoeira
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Cattle (calf)
-
Sheep (lamb)
-
Goat (kid)
-
Pig
-
Rabbit
-
Chicken
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Cattle (calf)
-
Meat and offal7day
-
-
Sheep (lamb)
-
Meat and offal7day
-
-
Goat (kid)
-
Meat and offal7day
-
-
Pig
-
Meat and offal7day
-
-
Rabbit
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Available in:
-
Portugal
Package description:
- Available only in Portuguese
- Available only in Portuguese
- Available only in Portuguese
- Available only in Portuguese
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Fixed combination application (Article 13b of Directive No 2001/82/EC)
Marketing authorisation holder:
- Huvepharma S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Huvepharma S.A.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 943/01/15NFVPT
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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Portuguese (PDF)
Published on: 19/04/2022