FDA
approval
· 2015-07-22
FDA Approved: NALTREXONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
Summary
The FDA approved a supplemental application for naltrexone hydrochloride from Sun Pharmaceutical Industries, Inc., updating an existing generic product.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for NALTREXONE HYDROCHLORIDE (NALTREXONE HYDROCHLORIDE)