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General MedicationsORALGeneric

FEMTRACE

ESTRADIOL ACETATE

Standard Dose
0.9MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview FEMTRACE is listed in Drugs@FDA under application 021633 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ESTRADIOL ACETATE Form and strength TABLET;ORAL - 0.9MG Sponsor APIL Submission history Latest submission status date: 2017-11-01 00:00:00.

Structured Monograph

Clinical summary

Approval overview FEMTRACE is listed in Drugs@FDA under application 021633 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ESTRADIOL ACETATE Form and strength TABLET;ORAL - 0.9MG Sponsor APIL Submission history Latest submission status date: 2017-11-01 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.