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Lannett Announces FDA Approval of NDA for Branded Anesthetic Product americanpharmaceuticalreview
January 17, 2020Lannett Company announced the U.S. Food and Drug Administration (FDA) has approved the New Drug Application (NDA), submitted under the 505(b)(2) regulatory pathway, for Cocaine Hydrochloride (HCl) Nasal Solution 4% (40 mg/mL) ...
Pharma Sources Insight July 2025
