Orospray

País: Irlanda

Língua: inglês

Origem: HPRA (Health Products Regulatory Authority)

Ingredientes ativos:

Chlortetracycline; Sulphanilamide

Disponível em:

Vetoquinol Ireland Limited

Código ATC:

QD06AA52

DCI (Denominação Comum Internacional):

Chlortetracycline; Sulphanilamide

Dosagem:

2.85, 50 gram/100gram

Forma farmacêutica:

Cutaneous spray, powder

Tipo de prescrição:

POM: Prescription Only Medicine as defined in relevant national legislation

Grupo terapêutico:

Cattle, Dogs, Goats, Horses, Sheep

Área terapêutica:

chlortetracycline, combinations

Indicações terapêuticas:

Antibacterial

Status de autorização:

Authorised

Data de autorização:

1988-10-11

Características técnicas

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Orospray
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Cutaneous spray, powder.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Horses, Cattle, Goat, Sheep and Dog.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the topical treatment of wounds infected by organisms sensitive to
the active ingredients.
For the prevention and treatment of post operative infections
following surgical procedures by topical application.
4.3 CONTRAINDICATIONS
Do not use in animals with known hypersensitivity to one of the
ingredients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
Each 100g powder contains :
Active substances:
Chlortetracycline (as hydrochloride) 2.850
g
Sulfanilamide
50.000 g
Excipients:
Methyl parahydroxybenzoate
0.115
g
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4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTION(S) FOR USE IN ANIMALS
Use of the product should be based on susceptibility testing of the
bacteria isolated from the animal. If this is not possible,
therapy should be based on local (regional, farm level)
epidemiological information about susceptibility of the target
bacteria.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE
MEDICINAL PRODUCT TO ANIMALS
Pressurised co