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General MedicationsORALGeneric

LORELCO

PROBUCOL

Standard Dose
250MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Discontinued
Summary

Approval overview LORELCO is listed in Drugs@FDA under application 017535 (NDA).

Review priority: PRIORITY Marketing status: Discontinued Active ingredient PROBUCOL Form and strength TABLET;ORAL - 250MG Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 1991-08-26 00:00:00.

Structured Monograph

Clinical summary

Approval overview LORELCO is listed in Drugs@FDA under application 017535 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient PROBUCOL Form and strength TABLET;ORAL - 250MG Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 1991-08-26 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.