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General MedicationsORALGeneric

NIMOTOP

NIMODIPINE

Standard Dose
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 NIMOTOP is listed in Drugs@FDA under application 018869 (NDA).

Review priority: PRIORITY Marketing status: Discontinued Active ingredient NIMODIPINE Form and strength CAPSULE;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor BAYER PHARMS Submission history Latest submission status date: 2006-01-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview NIMOTOP is listed in Drugs@FDA under application 018869 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient NIMODIPINE Form and strength CAPSULE;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor BAYER PHARMS Submission history Latest submission status date: 2006-01-20 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.