FDA Approved: NALOXONE HYDROCHLORIDE — Original Application (Somerset Therapeutics, LLC)

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Summary

FDA approved the original application for a generic naloxone hydrochloride product by Somerset Therapeutics, LLC (ANDA 207633).

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Diseases / indications

• Opioid Overdose

Drugs mentioned

• Naloxone Hydrochloride (Naloxone hydrochloride)

Snippet

ORIG AP for NALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE)