General MedicationsTOPICALGeneric
ESTRASORB
ESTRADIOL HEMIHYDRATE
Standard Dose
0.25%
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary
Approval overview ESTRASORB is listed in Drugs@FDA under application 021371 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient ESTRADIOL HEMIHYDRATE Form and strength EMULSION;TOPICAL - 0.25% Sponsor EXELTIS USA INC Submission history Latest submission status date: 2024-09-10 00:00:00.
Structured Monograph
Clinical summary
Approval overview ESTRASORB is listed in Drugs@FDA under application 021371 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ESTRADIOL HEMIHYDRATE Form and strength EMULSION;TOPICAL - 0.25% Sponsor EXELTIS USA INC Submission history Latest submission status date: 2024-09-10 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.