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Lupin gets USFDA nod for Cefdinir suspension

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Our Web Bureau Mumbai
Lupin gets USFDA nod for Cefdinir suspension
Our Web Bureau / Mumbai June 02, 2006
The US Food and Drug Administration (USFDA) has approved Lupin's abbreviated new drug application (ANDA) for Cefdinir suspension 125mg/5ml.

According to an official release issued to the BSE today, Cefdinir is a third generation cephalosporin administered orally to treat a wide variety of bacterial infections.

"The approval of our Cefdinir suspension and the recent approval for the capsule form by FDA reinforces Lupin

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First Published: Jun 02 2006 | 4:17 PM IST

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