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General MedicationsINJECTIONGeneric

FUDR

FLOXURIDINE

Standard Dose
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Discontinued
Summary

Approval overview FUDR is listed in Drugs@FDA under application 016929 (NDA).

Review priority: PRIORITY Marketing status: Discontinued Active ingredient FLOXURIDINE Form and strength INJECTABLE;INJECTION - 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HOSPIRA Submission history Latest submission status date: 1999-09-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview FUDR is listed in Drugs@FDA under application 016929 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient FLOXURIDINE Form and strength INJECTABLE;INJECTION - 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HOSPIRA Submission history Latest submission status date: 1999-09-20 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: PRIORITY

Interaction Notes

  • No interaction notes stored yet.
FUDR (FLOXURIDINE) | Drug Monograph | MedicHelpline