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 The leading web portal for pharmacy resources, news, education and careers November 22, 2017
Pharmacy Choice - Pharmaceutical News - Lannett Receives FDA Approval For Neomycin Sulfate Tablets USP, 500 mg - November 22, 2017

Pharmacy News Article

 7/1/16 - Lannett Receives FDA Approval For Neomycin Sulfate Tablets USP, 500 mg

By a News Reporter-Staff News Editor at Drug Week Lannett Company, Inc. (NYSE: LCI) announced that it has received approval from the U.S. Food and Drug Administration (FDA) of its Abbreviated New Drug Application (ANDA) for Neomycin Sulfate Tablets USP, 500 mg, the therapeutic equivalent to the reference listed drug, Neomycin Sulfate Tablets USP, 500 mg, of Teva Pharmaceuticals USA, Inc. According to IMS, total U.S. sales in 2015 of Neomycin Sulfate Tablets USP, 500 mg, at Average Wholesale Price (AWP) were approximately $3 million (see also Pharmaceutical Companies).

"The approval for Neomycin Sulfate Tablets expands our portfolio of anti-infective and antibiotic products and represents our fifth approval in 2016," said Arthur Bedrosian, chief executive officer of Lannett. "We expect to commence marketing the product in the next several months, adding to our positive momentum as we enter the coming fiscal year."

Keywords for this news article include: Antibiotics, Antiinfectives, Pharmaceutical Companies, Drugs, Therapy, Neomycin, FDA Actions, Aminoglycosides, Lannett Company Inc., Government Agencies Offices and Entities.

Our reports deliver fact-based news of research and discoveries from around the world. Copyright 2016, NewsRx LLC

(c) 2016 NewsRx LLC

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