Sulfaprime pó oral para administração na água de bebida para aves canoras, pombos-correio, coelhos anões, chinchilas e outros pequenos roedores (chinchilas, porquinhos-da-Índia, hamsters (cricetos), gerbilos, murganhos e ratos)
Sulfaprime pó oral para administração na água de bebida para aves canoras, pombos-correio, coelhos anões, chinchilas e outros pequenos roedores (chinchilas, porquinhos-da-Índia, hamsters (cricetos), gerbilos, murganhos e ratos)
Authorised
- Trimethoprim L-glutamate
- Sulfadimethoxine sodium
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Sulfaprime pó oral para administração na água de bebida para aves canoras, pombos-correio, coelhos anões, chinchilas e outros pequenos roedores (chinchilas, porquinhos-da-Índia, hamsters (cricetos), gerbilos, murganhos e ratos)
Active substance:
- Trimethoprim L-glutamate
- Sulfadimethoxine sodium
- Oxytetracycline hydrochloride
Target species:
-
Ornamental bird
-
Homing pigeon
-
Rabbit (non food-producing)
-
Hamster
-
Chinchilla
-
Guinea pig
-
Mouse
-
Gerbil
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Trimethoprim L-glutamate20.00/gram(s)1.00kilogram(s)
-
Sulfadimethoxine sodium100.00/gram(s)1.00kilogram(s)
-
Oxytetracycline hydrochloride150.00/gram(s)1.00kilogram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EQ09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- Available only in Portuguese
- Available only in Portuguese
- Available only in Portuguese
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoopan Produtos Pecuarios S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoopan Produtos Pecuarios S.A.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 504/01/12NFVPT
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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in another language below.
Portuguese (PDF)
Published on: 27/06/2022
