Salmocoli pó oral para administração na água de bebida para aves canoras, pombos-correio, coelhos anões e pequenos roedores (chinchilas, porquinhos-da-índia, hamsters (cricetos), gerbilos, murganhos
Salmocoli pó oral para administração na água de bebida para aves canoras, pombos-correio, coelhos anões e pequenos roedores (chinchilas, porquinhos-da-índia, hamsters (cricetos), gerbilos, murganhos
Authorised
- NEOMYCIN SULFATE
- Furazolidone
- Chloramphenicol
Product identification
Medicine name:
Salmocoli pó oral para administração na água de bebida para aves canoras, pombos-correio, coelhos anões e pequenos roedores (chinchilas, porquinhos-da-índia, hamsters (cricetos), gerbilos, murganhos
Active substance:
- NEOMYCIN SULFATE
- Furazolidone
- Chloramphenicol
Target species:
-
Homing pigeon
-
Rabbit (non food-producing)
-
Hamster
-
Ornamental bird
-
Chinchilla
-
Guinea pig
-
Gerbil
-
Mouse
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE30.00/gram(s)1.00kilogram(s)
-
Furazolidone30.00/gram(s)1.00kilogram(s)
-
Chloramphenicol30.00/gram(s)1.00kilogram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
Oral use
-
Homing pigeon
-
Rabbit (non food-producing)
-
Hamster
-
Ornamental bird
-
Chinchilla
-
Guinea pig
-
Gerbil
-
Mouse
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01BA01
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:
- 505/01/12NFVPT
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
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