FDA
approval
· 2024-08-13
FDA Approved: NALOXONE HYDROCHLORIDE — Supplemental Application (Hospira, Inc.)
Summary
FDA approved a supplemental application for Naloxone Hydrochloride by Hospira, Inc., under ANDA070256.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for NALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE)