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Zydus Cadila receives USFDA approval

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Capital Market

To market Levofloxacin

Zydus Cadila has announced that it has got approval from the United States Food and Drug Administration to market Levofloxacin Injection, 500 mg/20 ml, and 750 mg/30 ml (25 mg/ml), which is used in the treatment of bacterial infections. The product will be produced at the group's formulations manufacturing facility at Moraiya, Ahmedabad.

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First Published: Jun 02 2017 | 9:55 AM IST

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