Hikma FDA Thursday, February 25, 2010 0.00 Neutral

FDA Approves HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Hikma Pharmaceuticals USA Inc.

Hikma Pharmaceuticals USA Inc. announced the receipt of FDA approval for its Abbreviated New Drug Application (ANDA040881) for hydrocodone bitartrate and acetaminophen, enhancing its portfolio of generic narcotic pain relievers. This regulatory milestone strengthens Hikma's competitive position in the generic marketplace by expanding its distribution and revenue potential for widely utilized combination products.

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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