Երկիր: Միացյալ Թագավորություն
Լեզու: անգլերեն
Աղբյուրը: VMD (Veterinary Medicines Directorate)
Nitroscanate
Elanco Europe Ltd
QP52AX01
Nitroscanate
Film-coated tablet
AVM-GSL - Authorised Veterinary Medicine – General Sales List
Dogs
Anthelmintic
Expired
2000-06-30
Revised: November 2018 AN: 00829/2018 Page 1 of 4 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Beaphar One Dose Wormer for Dogs, 500 mg film coated tablets 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Active ingredient mg/tablet Nitroscanate 500 For a full list of excipients see section 6.1. 3. PHARMACEUTICAL FORM Film coated tablet. Yellowish-white to light beige round, film coated tablet, with ‘BCB’ imprinted on one side and ‘CGV’ on the other. 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Dogs. 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES A broad spectrum anthelmintic for use in dogs. It is highly effective in a single dose against common canine nematodes and cestodes in the UK: _Toxocara _ _canis, Toxascaris leonina, Ancylostoma caninum, Uncinaria stenocephala, Taenia _ _ovis, Taenia hydatigena, Taenia pisiformis _and_ Dipylidium caninum._ At the recommended dosage, the product gives limited control of _Echinococcus _ _granulosus._ 4.3 CONTRAINDICATIONS None. 4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES None. 4.5 SPECIAL PRECAUTIONS FOR USE i. Special precautions for use in animals Do not repeat treatment if vomiting occurs shortly after dosing. Revised: November 2018 AN: 00829/2018 Page 2 of 4 ii. Special precautions to be taken by the person administering the medicinal product to animals Tablets are film coated and should not be broken or divided. 4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS) The tablets, when administered as recommended are unlikely to cause vomiting. Do not repeat treatment if vomiting occurs shortly after dosing. 4.7 USE DURING PREGNANCY, LACTATION OR LAY Not contraindicated in pregnant animals. Nursing bitches should be treated at the same time and as frequently as puppies up to 12 weeks of age (i.e. 2, 4, 6, 8, 12 weeks). 4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION None known. 4.9 AMOUNT(S) TO BE ADMINISTERED AND ADMINISTRATION ROUTE For oral administration only. For the routine treatment of adult dogs Կարդացեք ամբողջական փաստաթուղթը