Aurobindo, USFDA and Cephalexin
Aurobindo Pharma gets USFDA nod to manufacture Cephalexin tablets
Aurobindo Pharma receives USFDA approval for Cephalexin tablets, expected to launch in Q3FY25 with CGT designation.
Aurobindo Pharma Receives US FDA Approval For An Antibiotics Tablet
Aurobindo Pharma has also been granted competitive generic therapy designation for these Cephalexin Tablets, qualifying the company for 180 days of shared generic drug exclusivity.
Aurobindo Pharma receives USFDA approval for Cephalexin Tablets
Aurobindo Pharma has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Cephalexin Tablets USP, 250 mg and 500 mg, which is bioequivalent and therapeutically equivalent to the reference listed drug (RLD),
Aurobindo Pharma secures FDA nod for Cephalexin tablets to treat infections
Hyderabad-headquartered Aurobindo Pharma has announced that it has received final approval from the U.S. Food and Drug Administration (USFDA) to manufacture and market Cephalexin Tablets USP in both 250 milligram (mg) and 500 mg dosages.
USFDA nod to Aurobindo Pharma for Cephalexin Tablets
Hyderabad: Aurobindo Pharma Limited has announced that it has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Cephalexin Tablets USP, 250 mg and
Aurobindo Pharma gets U.S. FDA nod for Cephalexin tablets
Aurobindo Pharma receives FDA approval for Cephalexin Tablets, bioequivalent to Keflet, with CGT designation and shared exclusivity.
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