Heron Therapeutics Announces FDA Approval Of Co.'s Prior Approval Supplement Application For ZYNRELEF Vial Access Needle
Portfolio Pulse from Benzinga Newsdesk
Heron Therapeutics has received FDA approval for its Prior Approval Supplement Application for the ZYNRELEF Vial Access Needle, which could enhance the product's marketability and usage.
September 25, 2024 | 12:06 pm
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Heron Therapeutics received FDA approval for its ZYNRELEF Vial Access Needle, which may improve the product's marketability and usage, potentially leading to increased sales and revenue.
The FDA approval is a positive regulatory development for Heron Therapeutics, likely enhancing the marketability of ZYNRELEF. This could lead to increased sales and revenue, positively impacting the stock price.
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