Gemcitabine 40mg/ml concentrate for solution for infusion - (25ml vial) Malta - engelsk - Medicines Authority

gemcitabine 40mg/ml concentrate for solution for infusion - (25ml vial)

fresenius kabi oncology plc lion court, farnham road, bordon, hampshire, gu35 0nf, united kingdom - gemcitabine hydrochloride - concentrate for solution for infusion - gemcitabine hydrochloride 40 mg - antineoplastic agents

Gemcitabine 40mg/ml concentrate for solution for infusion - (50ml vial) Malta - engelsk - Medicines Authority

gemcitabine 40mg/ml concentrate for solution for infusion - (50ml vial)

fresenius kabi oncology plc lion court, farnham road, bordon, hampshire, gu35 0nf, united kingdom - gemcitabine hydrochloride - concentrate for solution for infusion - gemcitabine hydrochloride 40 mg - antineoplastic agents

Gemcitabine 40 mg/ml concentrate for solution for Infusion Irland - engelsk - HPRA (Health Products Regulatory Authority)

gemcitabine 40 mg/ml concentrate for solution for infusion

fresenius kabi deutschland gmbh - gemcitabine - concentrate for solution for infusion - 40 milligram(s)/millilitre - pyrimidine analogues; gemcitabine

Gemcitabine Fresenius Kabi 40 mg/ml inf. sol. (conc.) i.v. vial Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

gemcitabine fresenius kabi 40 mg/ml inf. sol. (conc.) i.v. vial

fresenius kabi sa-nv - gemcitabine hydrochloride - eq. gemcitabine 40 mg/ml - concentrate for solution for infusion - 40 mg/ml - gemcitabine hydrochloride - gemcitabine

Gemcitabine Fresenius Kabi 40 mg/ml inf. sol. (conc.) i.v. vial Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

gemcitabine fresenius kabi 40 mg/ml inf. sol. (conc.) i.v. vial

fresenius kabi sa-nv - gemcitabine hydrochloride - eq. gemcitabine 40 mg/ml - concentrate for solution for infusion - 40 mg/ml - gemcitabine hydrochloride - gemcitabine

Gemcitabine Fresenius Kabi 40 mg/ml inf. sol. (conc.) i.v. vial Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

gemcitabine fresenius kabi 40 mg/ml inf. sol. (conc.) i.v. vial

fresenius kabi sa-nv - gemcitabine hydrochloride - eq. gemcitabine 40 mg/ml - concentrate for solution for infusion - 40 mg/ml - gemcitabine hydrochloride - gemcitabine

GEMCITABINE MEDAC 1500 MG Israel - engelsk - Ministry of Health

gemcitabine medac 1500 mg

tzamal bio-pharma ltd - gemcitabine as hydrochloride - powder for solution for infusion - gemcitabine as hydrochloride 1500 mg - gemcitabine - gemcitabine - palliative treatment of patients with locally advanced or metastatic non-small cell lung cancer and locallyadvanced or metastatic adenocarcinoma of the pancreas and for patients with 5-fu refractory pancreaticcancer.gemcitabine is indicated for the treatment of patients with bladder cancer at the invasive stage.breast cancer:gemcitabine in combination with paclitaxel is indicated for the treatment of patients with unresectable locallyrecurrent or metastatic breast cancer who have relapsed following adjuvant/neoadjuvant chemotherapy.prior chemotherapy should have included an anthracycline unless clinically contraindicated.ovarian cancer:gemcitabine in combination with carboplatin is indicated for the treatment of patients with recurrent epithelialovarian carcinoma whom have relapsed at least six months after platinum - based therapy.

GEMCITABINE TEVA  CONCENTRATE Israel - engelsk - Ministry of Health

gemcitabine teva concentrate

abic marketing ltd, israel - gemcitabine as hydrochloride - concentrate for solution for infusion - gemcitabine as hydrochloride 40 mg/ml - gemcitabine - gemcitabine - gemcitabine teva® concentrate is indicated for the palliative treatment of patients with locally advanced or metastatic non-small cell lung cancer and locally advanced or metastatic adenocarcinoma of the pancreas and for patients with 5-fu refractory pancreatic cancer.gemcitabine teva® concentrate is indicated for the treatment of patients with bladder cancer at the invasive stage.breast cancer:gemcitabine teva® concentrate in combination with paclitaxel,is indicated for the treatment of patients with unresectable, locally recurrent or metastatic breast cancer who have relapsed following adjuvant /neoadjuvant chemotherapy. prior chemotherapy should have included an anthracycline unless clinically contraindicated.ovarian cancer:gemcitabine teva® concentrate in combination with carboplatin, is indicated for the treatment of patients with recurrent epithelial ovarian carcinoma who have relapsed at least 6 months after platinum-based therapy.

GEMCITABINE injection USA - engelsk - NLM (National Library of Medicine)

gemcitabine injection

actavis pharma, inc. - gemcitabine hydrochloride (unii: u347pv74il) (gemcitabine - unii:b76n6sbz8r) - gemcitabine 38 mg in 1 ml - gemcitabine injection in combination with carboplatin is indicated for the treatment of patients with advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy. gemcitabine injection in combination with paclitaxel is indicated for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated. gemcitabine injection in combination with cisplatin is indicated for the first-line treatment of patients with inoperable, locally advanced (stage iiia or iiib) or metastatic (stage iv) non-small cell lung cancer (nsclc). gemcitabine injection is indicated as first-line treatment for patients with locally advanced (nonresectable stage ii or stage iii) or metastatic (stage iv) adenocarcinoma of the pancreas. gemcitabine injection is indicated for patients previously treated with fluorouracil. gemcitabine injection is contraindicated in patients with

GEMCITABINE HYDROCHLORIDE- gemcitabine hydrochloride injection, powder, lyophilized, for solution USA - engelsk - NLM (National Library of Medicine)

gemcitabine hydrochloride- gemcitabine hydrochloride injection, powder, lyophilized, for solution

heritage pharmaceuticals inc. - gemcitabine hydrochloride (unii: u347pv74il) (gemcitabine - unii:b76n6sbz8r) - gemcitabine 200 mg in 5 ml - gemcitabine in combination with carboplatin is indicated for the treatment of patients with advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy. gemcitabine in combination with paclitaxel is indicated for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated. gemcitabine is indicated in combination with cisplatin for the first-line treatment of patients with inoperable, locally advanced (stage iiia or iiib), or metastatic (stage iv) non-small cell lung cancer. gemcitabine is indicated as first-line treatment for patients with locally advanced (nonresectable stage ii or stage iii) or metastatic (stage iv) adenocarcinoma of the pancreas. gemcitabine is indicated for patients previously treated with 5-fu. gemcitabine for injection usp is contraindicated in patients with a known hypersensitivity to gemcitabine. pregnancy catego