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General MedicationsINJECTIONGeneric

FLOXURIDINE

FLOXURIDINE

Standard Dose
500MG/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview FLOXURIDINE is listed in Drugs@FDA under application 203008 (ANDA).

Marketing status: Discontinued Active ingredient FLOXURIDINE Form and strength INJECTABLE;INJECTION - 500MG/VIAL Sponsor AM REGENT Submission history Latest submission status date: 2017-11-22 00:00:00.

Structured Monograph

Clinical summary

Approval overview FLOXURIDINE is listed in Drugs@FDA under application 203008 (ANDA). Marketing status: Discontinued Active ingredient FLOXURIDINE Form and strength INJECTABLE;INJECTION - 500MG/VIAL Sponsor AM REGENT Submission history Latest submission status date: 2017-11-22 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.