Skip to main content
MedicHelpLine
Verified Professional Network190+ CountriesHIPAA-Aware Platform
Back to Drug Index
General MedicationsORALGeneric

MECLOMEN

MECLOFENAMATE SODIUM

Standard Dose
EQ 50MG BASE
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview MECLOMEN is listed in Drugs@FDA under application 018006 (NDA).

Marketing status: Discontinued Active ingredient MECLOFENAMATE SODIUM Form and strength CAPSULE;ORAL - EQ 50MG BASE Sponsor PARKE DAVIS Submission history Latest submission status date: 1990-07-23 00:00:00.

Structured Monograph

Clinical summary

Approval overview MECLOMEN is listed in Drugs@FDA under application 018006 (NDA). Marketing status: Discontinued Active ingredient MECLOFENAMATE SODIUM Form and strength CAPSULE;ORAL - EQ 50MG BASE Sponsor PARKE DAVIS Submission history Latest submission status date: 1990-07-23 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.