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General MedicationsORALGeneric

FEMCON FE

ETHINYL ESTRADIOL; NORETHINDRONE

Standard Dose
0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview FEMCON FE is listed in Drugs@FDA under application 021490 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ETHINYL ESTRADIOL; NORETHINDRONE Form and strength TABLET;ORAL - 0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor APIL Submission history Latest submission status date: 2017-08-09 00:00:00.

Structured Monograph

Clinical summary

Approval overview FEMCON FE is listed in Drugs@FDA under application 021490 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ETHINYL ESTRADIOL; NORETHINDRONE Form and strength TABLET;ORAL - 0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor APIL Submission history Latest submission status date: 2017-08-09 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
FEMCON FE (ETHINYL ESTRADIOL; NORETHINDRONE) | Drug Monograph | MedicHelpline