PAI FDA Friday, May 10, 2013 0.00 Neutral

FDA Approves HYDROCODONE BITARTRATE AND ACETAMINOPHEN — PAI Holdings, LLC dba PAI Pharma

PAI Holdings has secured FDA approval for its ANDA 040838, facilitating the market launch of hydrocodone bitartrate and acetaminophen, a widely utilized generic pain reliever. This expansion of the company’s product portfolio is expected to significantly bolster revenue streams and strengthen its competitive position within the generic opioid market.

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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