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Data updated: Mar 10, 2026

BIJUVA

ESTRADIOL Estrogen Receptor Agonists
Approved 2018-10-28
2
Indications
--
Phase 3 Trials
7
Years on Market

Details

Status
Prescription
First Approved
2018-10-28
Routes
ORAL
Dosage Forms
CAPSULE

Companies

Active Ingredient: ESTRADIOL , PROGESTERONE

BIJUVA Approval History

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What BIJUVA Treats

1 indications

BIJUVA is approved for 1 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Vasomotor Symptoms
Source: FDA Label

Drugs Similar to BIJUVA

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Shared indications:
Vasomotor Symptoms
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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

BIJUVA FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

BIJUVA is a combination of an estrogen and progesterone indicated in a woman with a uterus for the treatment of moderate to severe vasomotor symptoms due to menopause. 1.1 Treatment of Moderate to Severe Vasomotor Symptoms Due to Menopause

BIJUVA Patents & Exclusivity

Latest Patent: Nov 2032

Patents (78 active)

US10206932 Expires Nov 21, 2032
US8846649 Expires Nov 21, 2032
US8846648 Expires Nov 21, 2032
US9114146 Expires Nov 21, 2032
US9114145 Expires Nov 21, 2032
US10675288 Expires Nov 21, 2032
US9301920 Expires Nov 21, 2032
US11033626 Expires Nov 21, 2032
US9006222 Expires Nov 21, 2032
US10806740 Expires Nov 21, 2032
+ 68 more patents
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.