Lupin FDA Thursday, December 1, 2016 0.00 Neutral

FDA Approves HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Lupin Pharmaceuticals,Inc.

Lupin Pharmaceuticals announced on December 1, 2016, the FDA approval of hydrocodone bitartrate and acetaminophen tablets, an ANDA filing, expanding the generics landscape for a widely used opioid combination. This approval allows Lupin to introduce a cost-effective entry into the market, mimicking branded formulations and intensifying competitive pricing amidst ongoing skepticism regarding opioid utilization.

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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