Italy - English - myHealthbox

guna - roe extract, glycyrrhetinic acid , vitamin e , provitamin d , boswellia serrata, lecithin, zanthalene, calming agent (symsitive) - cream - aqua/water, octyldodecanol, cetearyl alcohol, caprylic/capric triglyceride, glycerin, alchol denat., ceteareth-20, glycyrrhetinic acid, oleyl alcohol, cetyl alcohol, zanthoxylum bungeanum fruit extract, pentylene glycol, 4-t-butyl-cyclohexanol, tocopherery - cosmetics

Kenya - English - Pharmacy and Poisons Board

norbrook kenya ltd old limuru road karuri p.o box 1287 00606 nairobi - oxytetracycline and flunixin - solution for injection - oxytetracycline 300mg/ml and flunixin 20mg/ml - non-steroidal

Israel - English - Ministry of Health

comex ltd - flunixin as meglumine 2 %w/v; oxytetracycline as dihydrate 30 %w/v - solution for injection - hexasol veterinary may be of use in the treatment of disease caused by microorgamisms sensitive to oxytetracycline where anti-inflammatory, anti-pyretic, and anti bacterial effect is required.

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

biotech laboratories (pty) ltd - injection - see ingredients - each 1,0 ml solution contains flunixin meglumine 20,0 mg oxytetracycline 300,0 mg

United States - English - NLM (National Library of Medicine)

norbrook laboratories limited - oxytetracycline (unii: x20i9en955) (oxytetracycline - unii:x20i9en955), flunixin meglumine (unii: 8y3jk0jw3u) (flunixin - unii:356ib1o400) - oxytetracycline 300 mg in 1 ml - for the treatment of bacterial pneumonia associated with pasteurella spp. and for the control of associated pyrexia in beef and non-lactating dairy cattle. do not use in animals showing hypersensitivity to either flunixin meglumine or oxytetracycline.

Uganda - English - National Drug Authority

norbrook laboratories ltd - oxytetracycline+flunixin - parenteral ordinary infusion vials/bottles - 300mg+20mg

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

norbrook laboratories australia pty limited - oxytetracycline as the dihydrate; flunixin as flunixin meglumine - parenteral liquid/solution/suspension - oxytetracycline as the dihydrate antibiotic active 300.0 mg/ml; flunixin as flunixin meglumine benzene active 20.0 mg/ml - antibiotic & related - cattle | beef | bos indicus | bos taurus | bovine | buffalo | bull | bullock | calf | cow | dairy cow | heifer | steer - bovine respiratory disease | organisms sensitive to oxytetracycline | enteric bacterial infection | respiratory infection | shipping fever

Saudi Arabia - English - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

norbrook laboratories ltd., ireland - oxytetracycline dihydrate, flunixin meglumine - solution for injection - 20.300 mg/ml

Saudi Arabia - English - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

norbrook laboratories ltd., ireland - oxytetracycline dihydrate, flunixin meglumine - solution for injection - 20.300 mg/ml

Australia - English - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - tramadol hydrochloride, quantity: 50 mg/ml - injection, solution - excipient ingredients: sodium acetate; water for injections - tramadol sandoz injections are indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.