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General MedicationsINTRAVENOUSGeneric

PARAPLATIN

CARBOPLATIN

Standard Dose
600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: UNKNOWN Marketing status: Discontinued
Summary

Approval overview PARAPLATIN is listed in Drugs@FDA under application 020452 (NDA).

Review priority: UNKNOWN Marketing status: Discontinued Active ingredient CARBOPLATIN Form and strength INJECTABLE;INTRAVENOUS - 600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor CORDENPHARMA Submission history Latest submission status date: 2010-11-05 00:00:00.

Structured Monograph

Clinical summary

Approval overview PARAPLATIN is listed in Drugs@FDA under application 020452 (NDA). Review priority: UNKNOWN Marketing status: Discontinued Active ingredient CARBOPLATIN Form and strength INJECTABLE;INTRAVENOUS - 600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor CORDENPHARMA Submission history Latest submission status date: 2010-11-05 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: UNKNOWN

Interaction Notes

  • No interaction notes stored yet.