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General MedicationsTRANSDERMALGeneric

ESTRADERM

ESTRADIOL

Standard Dose
0.05MG/24HR
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview ESTRADERM is listed in Drugs@FDA under application 019081 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ESTRADIOL Form and strength SYSTEM;TRANSDERMAL - 0.05MG/24HR Sponsor NOVARTIS Submission history Latest submission status date: 2017-11-01 00:00:00.

Structured Monograph

Clinical summary

Approval overview ESTRADERM is listed in Drugs@FDA under application 019081 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ESTRADIOL Form and strength SYSTEM;TRANSDERMAL - 0.05MG/24HR Sponsor NOVARTIS 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.