Actavis FDA Thursday, February 19, 2015 0.00 Neutral

FDA Approves BUPRENORPHINE — Actavis Pharma, Inc.

Actavis Pharma has received approval for the ANDA090819 filing, expanding its portfolio with this generic sublingual buprenorphine HCl product, a formulation expected to bolster its presence in the narcotic dependence treatment market while driving revenue through authorized generic pricing.

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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