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General MedicationsORALGeneric

DOLOBID

DIFLUNISAL

Standard Dose
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 DOLOBID is listed in Drugs@FDA under application 018445 (NDA).

Review priority: PRIORITY Marketing status: Discontinued Active ingredient DIFLUNISAL Form and strength TABLET;ORAL - 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor MERCK Submission history Latest submission status date: 2007-03-16 00:00:00.

Structured Monograph

Clinical summary

Approval overview DOLOBID is listed in Drugs@FDA under application 018445 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient DIFLUNISAL Form and strength TABLET;ORAL - 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor MERCK Submission history Latest submission status date: 2007-03-16 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
DOLOBID (DIFLUNISAL) | Drug Monograph | MedicHelpline