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Shilpa Medicare has received US Food and Drug
Administration final approval for its ANDA, Gemcitabine Injection, 200 mg/5.26 mL,
1 9/263 mL, and 2 g/52.6 mL (38 mg/mL) Single-dose vials on 04 October 2019.
Gemcitabine Injection, 200 mg/5.26 mL, 1 9/263 mL, and 2 g/52.6 mL
(38 mg/mL) is used in the treatment of Ovarian Cancer, Breast Cancer, Non-Small
Cell Lung Cancer and Pancreatic Cancer as recommended in the label approved by
FDA.
According to IQVIA MAT Q2 2019 data, the US market for Gemcitabine Injection,
38 mg/mL is approximately US$ 14.9 Million.
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