In a BSE filing on Monday, Cipla said, "It has received final approval for its abbreviated new drug application (ANDA) for Decitabine Injection 50 mg single-use sterile vial from the United States Food and Drug Administration (USFDA)."
The approved product is a generic equivalent of Otsuka America Pharmaceutical Inc's Dacogen. It is indicated f the treatment of patients with myelodysplastic syndromes (MDS), the company added.
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The company said the approved product is available for shipping immediately.
Cipla stock was trading 1.42 per cent lower at Rs 600 on the BSE.
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