Aurobindo Pharma gets USFDA nod for Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
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Hyderabad: Pharma major, Aurobindo Pharma Limited, today announced that the company has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 200 µg/50 mL and 400 µg/100 mL Single Dose flexible containers (Bags).
Aurobindo's Dexmedetomidine HCl in 0.9% Sodium Chloride Injection is a therapeutic equivalent generic version of Hospira's Precedex in 0.9% Sodium Chloride Injection. The product will be launched in January 2021.
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