Fluid transfer set, general-purpose Australia - English - Department of Health (Therapeutic Goods Administration)

fluid transfer set, general-purpose

grifols australia pty ltd - 43324 - fluid transfer set, general-purpose - disposable fluid transfer sets intended for the dosage/preparation of solutions using the gri-fill system.

Intravenous fluid container, single use Australia - English - Department of Health (Therapeutic Goods Administration)

intravenous fluid container, single use

grifols australia pty ltd - 35127 - intravenous fluid container, single use - gri-bags are disposable bags intended for solution dosage using the gri-fill system.

ANTICOAGULANT SODIUM CITRATE- trisodium citrate dihydrate solution United States - English - NLM (National Library of Medicine)

anticoagulant sodium citrate- trisodium citrate dihydrate solution

laboratorios grifols sa - trisodium citrate dihydrate (unii: b22547b95k) (anhydrous citric acid - unii:xf417d3psl) -

SODIUM CHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

sodium chloride injection, solution

laboratorios grifols sa - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698, sodium cation - unii:lyr4m0nh37) - sodium chloride 9 g in 1000 ml - sodium chloride injection, usp is indicated as a source of water and electrolytes. 0.9% sodium chloride injection, usp is also indicated for use as a priming solution in hemodialysis procedures. none known.

0.9% SODIUM CHLORIDE INJECTION, USP SOLUTION Canada - English - Health Canada

0.9% sodium chloride injection, usp solution

laboratorios grifols s.a. - sodium chloride - solution - 0.9% - sodium chloride 0.9%

TERBINAFINE LICONSA 250 Milligram Tablets Ireland - English - HPRA (Health Products Regulatory Authority)

terbinafine liconsa 250 milligram tablets

laboratorios liconsa, s.a. - terbinafine - tablets - 250 milligram - antifungals for systemic use - antifungals for systemic use - it is indicated in the treatment of the following skin and nail fungal infections: treatment of tinea corporis, tinea cruris and tinea pedis, when oral therapy is considered appropriate depending on the site, severity or extent of the infection and for the treatment of onychomycosis caused by dermatophytes

Hiprabovis IBR Marker Live European Union - English - EMA (European Medicines Agency)

hiprabovis ibr marker live

laboratorios hipra s.a - live ge- tk- double-gene-deleted bovine herpes virus type 1, strain ceddel: 106.3–107.3 ccid50 - immunologicals - cattle - for the active immunisation of cattle from three months of age against bovine herpes virus type 1 (bohv-1) to reduce the clinical signs of infectious bovine rhinotracheitis (ibr) and field virus excretion.onset of immunity: 21 days after completion of the basic vaccination scheme.duration of immunity: 6 months after completion of the basic vaccination scheme

Rhiniseng European Union - English - EMA (European Medicines Agency)

rhiniseng

laboratorios hipra s.a. - inactivated bordetella bronchiseptica, strain 833cer / recombinant type-d pasteurella-multocida toxin (pmtr) - immunologicals - pigs (gilts and sows) - for the passive protection of piglets via colostrum after active immunisation of sows and gilts to reduce the clinical signs and lesions of progressive and non-progressive atrophic rhinitis, as well as to reduce weight loss associated with bordetella-bronchiseptica and pasteurella-multocida infections during the fattening period. challenge studies have demonstrated that passive immunity lasts until piglets are six weeks of age while in clinical field trials, the beneficial effects of vaccination (reduction in nasal lesion score and weight loss) are observed until slaughter.

Startvac European Union - English - EMA (European Medicines Agency)

startvac

laboratorios hipra s.a. - escherichia coli j5 inactivated, staphylococcus aureus (cp8) strain sp 140 inactivated, expressing slime-associated antigenic complex - immunologicals for bovidae - cattle (cows and heifers) - for herd immunisation of healthy cows and heifers, in dairy cattle herds with recurring mastitis problems, to reduce the incidence of sub-clinical mastitis and the incidence and the severity of the clinical signs of clinical mastitis caused by staphylococcus aureus, coliforms and coagulase-negative staphylococci.the full immunisation scheme induces immunity from approximately day 13 after the first injection until approximately day 78 after the third injection (equivalent to 130 days post-parturition).

SELECTAN SOLUTION FOR INJECTION FOR CATTLE AND PIGS Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

selectan solution for injection for cattle and pigs

laboratorios hipra s.a. - florfenicol - parenteral liquid/solution/suspension - florfenicol antibiotic active 300.0 mg/ml - antibiotic & related