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16 April, 2024 16:29 IST
Lupin receives USFDA approval for Decitabine for injection
Source: IRIS | 15 Nov, 2018, 12.00PM
Rating: NAN / 5 stars.
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Pharma major Lupin announced that it has received approval for its Decitabine for Injection, 50 mg/vial, Single-Dose Vial from the United States Food and Drug Administration (FDA) to market a generic version of Otsuka Pharmaceutical (Otsuka) Dacogen for Injection, 50 mg/vial, Single-Dose Vial.

Lupin's Decitabine for Injection, 50 mg/vial, Single-Dose Vial is the generic version of Otsuka's Dacogen for Injection, 50 mg/vial, Single-Dose Vial. It is indicated for the treatment of patients with myelodysplastic syndromes (MDS) including previously treated and untreated, de novo and secondary MDS of all French-American-British subtypes (refractory anemia, refractory anemia with ringed sideroblasts, refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, and chronic myelomonocytic leukemia) and intermediate-1, intermediate-2, and high-risk International Prognostic Scoring System groups.

Decitabine for Injection, 50 mg/vial, Single-Dose Vial had annual sales of approximately USD 135.9 million in the US (IQVIA MAT September 2018).

Shares of the company gained Rs 7, or 0.83%, to trade at Rs 848.30. The total volume of shares traded was 25,357 at the BSE (11.53 a.m., Thursday).

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