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General MedicationsORALGeneric

FLUMADINE

RIMANTADINE HYDROCHLORIDE

Standard Dose
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 FLUMADINE is listed in Drugs@FDA under application 019649 (NDA).

Review priority: PRIORITY Marketing status: Discontinued Active ingredient RIMANTADINE HYDROCHLORIDE Form and strength TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SUN PHARM INDS INC Submission history Latest submission status date: 2015-10-19 00:00:00.

Structured Monograph

Clinical summary

Approval overview FLUMADINE is listed in Drugs@FDA under application 019649 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient RIMANTADINE HYDROCHLORIDE Form and strength TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SUN PHARM INDS INC Submission history Latest submission status date: 2015-10-19 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued
  • Review priority: PRIORITY

Interaction Notes

  • No interaction notes stored yet.
FLUMADINE (RIMANTADINE HYDROCHLORIDE) | Drug Monograph | MedicHelpline