GEMCITABINE HYDROCHLORIDE injection powder lyophilized for solution Stati Uniti - inglese - NLM (National Library of Medicine)

gemcitabine hydrochloride injection powder lyophilized for solution

watson laboratories, inc. - gemcitabine hydrochloride (unii: u347pv74il) (gemcitabine - unii:b76n6sbz8r) - gemcitabine 200 mg in 5 ml

GEMCITABINE HYDROCHLORIDE injection powder lyophilized for solution Stati Uniti - inglese - NLM (National Library of Medicine)

gemcitabine hydrochloride injection powder lyophilized for solution

pfizer laboratories div pfizer inc. - gemcitabine hydrochloride (unii: u347pv74il) (gemcitabine - unii:b76n6sbz8r) - gemcitabine 200 mg in 5 ml

GEMCITABINE ACTAVIS 200 gemcitabine 200 mg (as hydrochloride) powder for injection vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

gemcitabine actavis 200 gemcitabine 200 mg (as hydrochloride) powder for injection vial

medis pharma pty ltd - gemcitabine hydrochloride, quantity: 228 mg (equivalent: gemcitabine, qty 200 mg) - injection, powder for - excipient ingredients: mannitol; sodium hydroxide; sodium acetate trihydrate - treatment of patients with locally advanced or metastatic non-small cell lung cancer. treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. treatment of patients with fu refractory pancreatic cancer. treatment of patients with bladder cancer, alone or in combination with cisplatin. treatment, in combination with paclitaxel, 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. treatment, in combination with carboplatin, of patients with recurrent epithelial ovarian carcinoma, who have relapsed >six months following platinum based therapy.

DBL GEMCITABINE INJECTION gemcitabine (as hydrochloride) 2g/52.6mL solution for Injection vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

dbl gemcitabine injection gemcitabine (as hydrochloride) 2g/52.6ml solution for injection vial

pfizer australia pty ltd - gemcitabine hydrochloride, quantity: 2.277 g - injection, solution - excipient ingredients: water for injections; hydrochloric acid; sodium hydroxide - dbl gemcitabine injection is indicated: 1. for treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc). 2. for treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. 3. for treatment of patients with fu refractory pancreatic cancer. 4. alone or in combination with cisplatin, is indicated for treatment of patients with bladder cancer. 5. in combination with paclitaxel, 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. 6. in combination with carboplatin, for the treatment of patients with recurrent epithelial ovarian carcinoma, who have relapsed > 6 months following platinum-based therapy.

GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 2000 mg/50 mL concentrated solution for infusion vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

gemcitabine sandoz gemcitabine (as hydrochloride) 2000 mg/50 ml concentrated solution for infusion vial

sandoz pty ltd - gemcitabine hydrochloride, quantity: 2278 mg (equivalent: gemcitabine, qty 2000 mg) - injection, concentrated - excipient ingredients: dilute hydrochloric acid; water for injections - treatment of patients with locally advanced or metastatic non-small cell lung cancer. ? treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. ? treatment of patients with 5fu refractory pancreatic cancer. ? treatment of patients with bladder cancer, alone or in combination with cisplatin. ? treatment, in combination with paclitaxel, 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. ? treatment, in combination with carboplatin, of patients with recurrent epithelial ovarian carcinoma, who have relapsed > six months following platinum based therapy.

GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 200 mg/5 mL concentrated solution for infusion vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

gemcitabine sandoz gemcitabine (as hydrochloride) 200 mg/5 ml concentrated solution for infusion vial

sandoz pty ltd - gemcitabine hydrochloride, quantity: 227.8 mg (equivalent: gemcitabine, qty 200 mg) - injection, concentrated - excipient ingredients: dilute hydrochloric acid; water for injections - treatment of patients with locally advanced or metastatic non-small cell lung cancer. ? treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. ? treatment of patients with 5fu refractory pancreatic cancer. ? treatment of patients with bladder cancer, alone or in combination with cisplatin. ? treatment, in combination with paclitaxel, 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. ? treatment, in combination with carboplatin, of patients with recurrent epithelial ovarian carcinoma, who have relapsed > six months following platinum based therapy.

GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 1000 mg/25 mL concentrated solution for infusion vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

gemcitabine sandoz gemcitabine (as hydrochloride) 1000 mg/25 ml concentrated solution for infusion vial

sandoz pty ltd - gemcitabine hydrochloride, quantity: 1139 mg (equivalent: gemcitabine, qty 1000 mg) - injection, concentrated - excipient ingredients: water for injections; dilute hydrochloric acid - ? treatment of patients with locally advanced or metastatic non-small cell lung cancer. ? treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. ? treatment of patients with 5fu refractory pancreatic cancer. ? treatment of patients with bladder cancer, alone or in combination with cisplatin. ? treatment, in combination with paclitaxel, 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. ? treatment, in combination with carboplatin, of patients with recurrent epithelial ovarian carcinoma, who have relapsed > six months following platinum based therapy.

DBL GEMCITABINE INJECTION gemcitabine (as hydrochloride) 1g/26.3mL solution for Injection vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

dbl gemcitabine injection gemcitabine (as hydrochloride) 1g/26.3ml solution for injection vial

pfizer australia pty ltd - gemcitabine hydrochloride, quantity: 1.139 g - injection, solution - excipient ingredients: hydrochloric acid; sodium hydroxide; water for injections - dbl gemcitabine injection is indicated: 1. for treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc). 2. for treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. 3. for treatment of patients with fu refractory pancreatic cancer. 4. alone or in combination with cisplatin, is indicated for treatment of patients with bladder cancer. 5. in combination with paclitaxel, 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. 6. in combination with carboplatin, for the treatment of patients with recurrent epithelial ovarian carcinoma, who have relapsed > 6 months following platinum-based therapy.

DBL GEMCITABINE INJECTION gemcitabine (as hydrochloride) 200mg/5.3mL solution for Injection vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

dbl gemcitabine injection gemcitabine (as hydrochloride) 200mg/5.3ml solution for injection vial

pfizer australia pty ltd - gemcitabine hydrochloride, quantity: 227.7 mg - injection, solution - excipient ingredients: water for injections; hydrochloric acid; sodium hydroxide - dbl gemcitabine injection is indicated: 1. for treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc). 2. for treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. 3. for treatment of patients with fu refractory pancreatic cancer. 4. alone or in combination with cisplatin, is indicated for treatment of patients with bladder cancer. 5. in combination with paclitaxel, 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. 6. in combination with carboplatin, for the treatment of patients with recurrent epithelial ovarian carcinoma, who have relapsed > 6 months following platinum-based therapy.

GEMCITABINE injection Stati Uniti - inglese - 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