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General MedicationsINTRAVENOUSGeneric

ELOXATIN

OXALIPLATIN

Standard Dose
100MG/20ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: STANDARD Marketing status: Discontinued
Summary

Approval overview ELOXATIN is listed in Drugs@FDA under application 021759 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient OXALIPLATIN Form and strength INJECTABLE;INTRAVENOUS - 100MG/20ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2023-06-23 00:00:00.

Structured Monograph

Clinical summary

Approval overview ELOXATIN is listed in Drugs@FDA under application 021759 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient OXALIPLATIN Form and strength INJECTABLE;INTRAVENOUS - 100MG/20ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2023-06-23 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.