Rumænien - rumænsk - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

linde gaz romania s.r.l. - romania - oxigenum - gaz medicinal, comprimat - 100%(v/v) - alte preparate terapeutice gaze medicinale

Slovakiet - slovakisk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

linde gas s.r.o., slovensko - kyslík - 87 - varia i

Moldova - rumænsk - ANSA (Agenţia Naţională pentru Siguranţa Alimentelor)

agrobioprom, rusia - fluvalinat - benzi impregnate - albine

Moldova - rumænsk - ANSA (Agenţia Naţională pentru Siguranţa Alimentelor)

sc romvac company sa, românia - bromadiolonă, - şobolani, şoareci

Moldova - rumænsk - ANSA (Agenţia Naţională pentru Siguranţa Alimentelor)

sc promark trade srl, românia - premix - pulbere - animale mari și mici, păsări

Australien - engelsk - APVMA (Australian Pesticides and Veterinary Medicines Authority)

bioniche - gentamicin as sulfate(3000iu/g)+clotrimazole(10mg/g) + others - topical cream, ointment, paste, gel, lotion - antibiotic,antifungal - dog | bitch | castrate | puppy - anti-infective or antiseptic | malassezia pachydermatis | otitis externa | acute canine otitis | associated with yeast &/or bac | bacterial infections | chronic canine otitis | conjunctivitis | eye infections | eye-washes | keratoconjunctivitis | malassezia pachydermatis | ocular infections | otitis (canine) | pityrosporum pachydermatis | seborrhoeic dermatitis

Den Europæiske Union - dansk - EMA (European Medicines Agency)

crealta pharmaceuticals ireland limited - pegloticase - gigt - antigout præparater - krystexxa er indiceret til behandling af svær invaliderende kroniske tophaceous gigt i voksne patienter der kan have erosive fælles engagement og der har ikke kunnet normalisere serum urinsyre med xanthin oxidase hæmmere på maksimalt lægeligt passende dosis eller for hvem disse lægemidler er kontraindiceret.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

teva b.v.  - lamivudin - hiv infektioner - antivirale midler til systemisk anvendelse - lamivudin teva pharma b. indikeres som en del af antiretroviral kombinationsbehandling til behandling af humane immunsvigt-virus (hiv) -inficerede voksne og børn.

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - oestradiol; oestradiol hemihydrate -

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

juno pharmaceuticals pty ltd - estradiol hemihydrate, quantity: 0.77 mg (equivalent: estradiol, qty 0.75 mg) - drug delivery system, transdermal - excipient ingredients: isopropyl palmitate; polyethylene terephthalate; ethyl acetate; acrylic acid; 2-ethylhexyl acrylate; methyl acrylate; glycidyl methacrylate; 2,2'-azobisisobutyronitrile; hexane - menopausal symptoms: short-term treatment of signs and symptoms of oestrogen deficiency due to menopause, whether natural or surgically induced. in women with an intact uterus, oestrogen should always be opposed by progestogen in an adequate dosage regimen to ensure secretory transformation of the endometrium at regular intervals (refer to section 5.1 pharmacodynamic properties - clinical trials and section 4.2 dose and method of administration). estraderm mx 25 is not indicated for the prevention of post-menopausal bone mineral density loss. combination hrt should not be used in hysterectomised women because it is not needed in these women and it may increase risk of breast cancer