Evrópusambandið - franska - EMA (European Medicines Agency)

dompé biotec s.p.a. - darbepoetin alfa - kidney failure, chronic; anemia; cancer - préparations antianémiques - traitement de l'anémie symptomatique associée à l'insuffisance rénale chronique (irc) chez les adultes et les patients pédiatriques. traitement de l'anémie symptomatique chez les adultes chez les patients avec cancer non myéloïde recevant une chimiothérapie.

Írland - enska - HPRA (Health Products Regulatory Authority)

colgate-palmolive (u.k.) ltd - sodium fluoride - toothpaste - 5000 ppm - caries prophylactic agents

Írland - enska - HPRA (Health Products Regulatory Authority)

colgate-palmolive a/s - sodium fluoride - toothpaste - 5000 ppm - caries prophylactic agents; sodium fluoride

Austurríki - þýska - AGES (Agentur für Gesundheit und Ernährungssicherheit)

ever valinject gmbh - bortezomib -

Þýskaland - þýska - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

acadicpharm gmbh (8055934) - gemcitabinhydrochlorid - pulver zur herstellung einer infusionslösung - teil 1 - pulver zur herstellung einer infusionslösung; gemcitabinhydrochlorid (27608) 1140 milligramm

Ástralía - enska - APVMA (Australian Pesticides and Veterinary Medicines Authority)

wsd agribusiness pty ltd - rotenone from derris; magnesium fluorosilicate; sulfur - topical solution/suspension - rotenone from derris extract-plant active 13.0 g/kg; magnesium fluorosilicate mineral-fluorine active 400.0 g/kg; sulfur mineral-sulfur active 250.0 g/kg - parasiticides - sheep - off shears | sheep short wool (shorn) | ovine | sheep - off shears | sheep - shorn - sheep body louse | sheep face louse | sheep foot louse | sheep itch mite | sheep ked | damalinia ovis (prev. genus) | lice - synthetic pyrethroid re | psorobia ovis | sheep body lice

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - idarubicin hydrochloride, quantity: 1 mg/ml - injection, concentrated - excipient ingredients: glycerol; water for injections; sodium hydroxide; dilute hydrochloric acid - idarubicin ebewe is indicated for use in acute myelogenous leukaemia (aml) in adults for remission induction in untreated patients or for remission induction in relapsed or refractory patients. idarubicin ebewe may be used in combination chemotherapy regimens involving other cytotoxic agents.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - idarubicin hydrochloride, quantity: 1 mg/ml - injection, concentrated - excipient ingredients: glycerol; dilute hydrochloric acid; water for injections; sodium hydroxide - idarubicin ebewe is indicated for use in acute myelogenous leukaemia (aml) in adults for remission induction in untreated patients or for remission induction in relapsed or refractory patients. idarubicin ebewe may be used in combination chemotherapy regimens involving other cytotoxic agents.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - idarubicin hydrochloride, quantity: 1 mg/ml - injection, concentrated - excipient ingredients: sodium hydroxide; water for injections; dilute hydrochloric acid; glycerol - idarubicin ebewe is indicated for use in acute myelogenous leukaemia (aml) in adults for remission induction in untreated patients or for remission induction in relapsed or refractory patients. idarubicin ebewe may be used in combination chemotherapy regimens involving other cytotoxic agents.

Þýskaland - þýska - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

lapharm gmbh pharmazeutische produkte (8151862) - carboplatin - konzentrat zur herstellung einer infusionslösung - teil 1 - konzentrat zur herstellung einer infusionslösung; carboplatin (23168) 10 milligramm