Actavis FDA Tuesday, January 21, 1997 0.00 Neutral

FDA Approves PENTAZOCINE AND NALOXONE — Actavis Pharma, Inc.

Actavis Pharma has received approval for the Abbreviated New Drug Application (ANDA #074736) to market Pentazocine Hydrochloride, a generic oral formulation of the compound originally approved in 1997. The expanded distribution is expected to bolster Actavis's market presence in the opioid analgesic sector, providing a cost-effective alternative to the brand-name product.

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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