GeoPharma Gets FDA Aprroval For Cephalosporin Plant In Florida
GeoPharma has also indicated that, based on the adequacy of its written response, it is acceptable to manufacture upon FDA approval of its Cephalexin ANDA. Mihir Taneja, CEO
The US Food and Drug Administration (FDA) is set to review Kowa Pharmaceuticals America’s new drug application (NDA) for K-911, an investigational once-daily eye drop aimed at reducing intraocular pressure (IOP) in open-angle glaucoma (OAG) or ocular hypertension (OHT) patients.