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General MedicationsORALGeneric

ANZEMET

DOLASETRON MESYLATE

Standard Dose
100MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: 901 REQUIRED Marketing status: Discontinued
Summary

Approval overview ANZEMET is listed in Drugs@FDA under application 020623 (NDA).

Review priority: 901 REQUIRED Marketing status: Discontinued Active ingredient DOLASETRON MESYLATE Form and strength TABLET;ORAL - 100MG Sponsor VALIDUS PHARMS Submission history Latest submission status date: 2014-09-18 00:00:00.

Structured Monograph

Clinical summary

Approval overview ANZEMET is listed in Drugs@FDA under application 020623 (NDA). Review priority: 901 REQUIRED Marketing status: Discontinued Active ingredient DOLASETRON MESYLATE Form and strength TABLET;ORAL - 100MG Sponsor VALIDUS PHARMS Submission history Latest submission status date: 2014-09-18 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: 901 REQUIRED

Interaction Notes

  • No interaction notes stored yet.