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General MedicationsINJECTIONGeneric

PROGESTERONE

PROGESTERONE

Standard Dose
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 PROGESTERONE is listed in Drugs@FDA under application 017362 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient PROGESTERONE Form and strength INJECTABLE;INJECTION - 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ACTAVIS LABS UT INC Submission history Latest submission status date: 2018-08-21 00:00:00.

Structured Monograph

Clinical summary

Approval overview PROGESTERONE is listed in Drugs@FDA under application 017362 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient PROGESTERONE Form and strength INJECTABLE;INJECTION - 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ACTAVIS LABS UT INC Submission history Latest submission status date: 2018-08-21 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
PROGESTERONE (PROGESTERONE) | Drug Monograph | MedicHelpline