Aurobindo receives US FDA approval to sell Cefdinir in US

Aurobindo Pharma Ltd has received an approval from the USFDA to market its 300mg cefdinir capsules in the US market. This is company's 62nd ANDA approval. The drug falls under the anti-bacterial segment and is a generic equivalent of Abbott Laboratories' Omnicef. Earlier, the company also received the final approval for 125 mg/5 mL and 250 mg/5 mL oral suspension of this drug from the US FDA.