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General MedicationsORALGeneric

ANTARA (MICRONIZED)

FENOFIBRATE

Standard Dose
87MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview ANTARA (MICRONIZED) is listed in Drugs@FDA under application 021695 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient FENOFIBRATE Form and strength CAPSULE;ORAL - 87MG Sponsor LUPIN Submission history Latest submission status date: 2025-10-01 00:00:00.

Structured Monograph

Clinical summary

Approval overview ANTARA (MICRONIZED) is listed in Drugs@FDA under application 021695 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FENOFIBRATE Form and strength CAPSULE;ORAL - 87MG Sponsor LUPIN Submission history Latest submission status date: 2025-10-01 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
ANTARA (MICRONIZED) (FENOFIBRATE) | Drug Monograph | MedicHelpline