Gemcitabine 1000 Mg, Powder for Solution for Infusion
Qualitative and Quantitative Composition
Each Vial Contains 1000 Mg Gemcitabine (as Hydrochloride)
Excipients With Known Effect:
Each Vial Contains 17.5 Mg Sodium.
One Ml of the Reconstituted Solution for Infusion Contains 38 Mg Gemcitabine (as Hydrochloride).
Powder for Solution Infusion.
White to Off-white Lyophilized Cake.
Gemcitabine Is Indicated for the Treatment of Locally Advanced or Metastatic Bladder Cancer in Combination With Cisplatin.
Gemcitabine Is Indicated for Treatment of Patients With Locally Advanced or Metastatic Adenocarcinoma of the Pancreas.
Gemcitabine, in Combination With Cisplatin Is Indicated as First Line Treatment of Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer (Nsclc). Gemcitabine Monotherapy Can Be Considered in Elderly Patients or Those With Performance Status 2.
Gemcitabine Is Indicated for the Treatment of Patients With Locally Advanced or Metastatic Epithelial Ovarian Carcinoma, in Combination With Carboplatin, in Patients With Relapsed Disease Following a Recurrence-free Interval of at Least 6 Months After Platinum-based, First-line Therapy.
Gemcitabine, 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.