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General MedicationsINJECTIONGeneric

NALOXONE HYDROCHLORIDE

NALOXONE HYDROCHLORIDE

Standard Dose
0.02MG/ML
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview NALOXONE HYDROCHLORIDE is listed in Drugs@FDA under application 072085 (ANDA).

Marketing status: Discontinued Active ingredient NALOXONE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 0.02MG/ML Sponsor IGI LABS INC Submission history See approval history documents.

Structured Monograph

Clinical summary

Approval overview NALOXONE HYDROCHLORIDE is listed in Drugs@FDA under application 072085 (ANDA). Marketing status: Discontinued Active ingredient NALOXONE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 0.02MG/ML Sponsor IGI LABS INC Submission history See approval history documents.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.