Strides receives USFDA approval for generic flucytosine capsules

Strides receives USFDA approval for generic flucytosine capsules

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Medicine
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Strides Pharma Science has announced that its step-down wholly owned subsidiary, Strides Pharma Global Pte. Singapore, has received approval for flucytosine capsules USP, 250 mg and 500 mg from the United States Food & Drug Administration (FDA). The product is a generic version of Ancobon capsules, 250 mg and 500 mg, of Bausch Health US, LLC.

According to IQVIA MAT data, the US market for flucytosine capsules USP, 250 mg and 500 mg is approximately US$ 45 million. The product will be manufactured at the company’s flagship facility at Bengaluru and will be marketed by Strides Pharma Inc. in the US market.

Also read: Zydus gets USFDA approval for baclofen tablets

The company has 123 cumulative ANDA filings with US FDA of which 86 ANDAs have been approved and 37 are pending approval.

Flucytosine capsule is indicated only in the treatment of serious infections caused by susceptible strains of Candida (septicemia, endocarditis and urinary system infections) and/or cryptococcus (meningitis and pulmonary infections).