Aurolife FDA Monday, April 15, 2013 0.00 Neutral

FDA Approves ACETAMINOPHEN AND CODEINE PHOSPHATE — Aurolife Pharma, LLC

On April 15, 2013, Aurolife Pharma, LLC received FDA approval for the ANDA representing acetaminophen and codeine phosphate tablets. This authorization strengthens the market offering of this widely used analgesic by adding a generic alternative and providing a potential boost to the company's product portfolio.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

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