US FDA approval Orchid's ANDA for Cefpodoxime Proxetil

17 Nov 2007

1

The US FDA has approved the Chennai-based Orchid Chemicals & Pharmaceuticals Ltd abbreviated new drug application (ANDA) for Cefpodoxime Proxetil Tablets.  

The product is available in two dosage strengths, 100 mg and 200 mg.

Cefpodoxime Proxetil is a 3rd generation cephalosporin antibiotic which has a broad spectrum activity against organisms causing infectious diseases.

With limited generic competition in this product, Orchid hopes to acquire a sizeable market share and revenues in the US market.

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