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General MedicationsINJECTIONGeneric

OXACILLIN SODIUM

OXACILLIN SODIUM

Standard Dose
EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview OXACILLIN SODIUM is listed in Drugs@FDA under application 050195 (NDA).

Marketing status: Discontinued Active ingredient OXACILLIN SODIUM Form and strength INJECTABLE;INJECTION - EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor APOTHECON Submission history See approval history documents.

Structured Monograph

Clinical summary

Approval overview OXACILLIN SODIUM is listed in Drugs@FDA under application 050195 (NDA). Marketing status: Discontinued Active ingredient OXACILLIN SODIUM Form and strength INJECTABLE;INJECTION - EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor APOTHECON Submission history See approval history documents.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.