Elite Pharma plans FDA ANDA filing after bioequivalence study for anticonvulsant generic

ELITE PHARMACEUTICALS INC

ELITE PHARMACEUTICALS INC

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  • Elite reported positive pivotal bioequivalence results for an undisclosed anticonvulsant generic, clearing the way for an FDA ANDA filing.
  • IQVIA data cited sales of $840 million for branded and generic versions in the 12 months ended April 2026.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Elite Pharmaceuticals Inc. published the original content used to generate this news brief via Newsfile (Ref. ID: 202606150700NEWSFILECNPR____20260615_301416_1) on June 15, 2026, and is solely responsible for the information contained therein.

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