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General MedicationsINTRAMUSCULAR, SUBCUTANEOUSGeneric

NALOXONE HYDROCHLORIDE (AUTOINJECTOR)

NALOXONE HYDROCHLORIDE

Standard Dose
10MG/0.4ML (10MG/0.4ML)
Max Dose
Refer to approved labeling
Primary Use
Review priority: N/A Marketing status: Discontinued
Summary

Approval overview NALOXONE HYDROCHLORIDE (AUTOINJECTOR) is listed in Drugs@FDA under application 215457 (NDA).

Review priority: N/A Marketing status: Discontinued Active ingredient NALOXONE HYDROCHLORIDE Form and strength SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - 10MG/0.4ML (10MG/0.4ML) Sponsor KALEO INC Submission history Latest submission status date: 2023-04-03 00:00:00.

Structured Monograph

Clinical summary

Approval overview NALOXONE HYDROCHLORIDE (AUTOINJECTOR) is listed in Drugs@FDA under application 215457 (NDA). Review priority: N/A Marketing status: Discontinued Active ingredient NALOXONE HYDROCHLORIDE Form and strength SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - 10MG/0.4ML (10MG/0.4ML) Sponsor KALEO INC Submission history Latest submission status date: 2023-04-03 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: N/A

Interaction Notes

  • No interaction notes stored yet.