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Progesterone vaginal tablet

Vastra Gotaland Region · FDA-approved active Small molecule ✓ Verified May 2026 Quality 2/100

Progesterone vaginal tablet is a Small molecule drug developed by Vastra Gotaland Region. It is currently FDA-approved. Also known as: Lutinus, manufactured by Ferring GmbH. ATC code G03DA04.

Progesterone vaginal tablets are a type of small molecule medication that acts as a progesterone receptor agonist. They are used to treat various conditions, including fertility issues, embryo implantation, and endometrial hyperplasia, as well as to support frozen embryo transfer.

At a glance

Generic nameProgesterone vaginal tablet
Also known asLutinus, manufactured by Ferring GmbH. ATC code G03DA04
SponsorVastra Gotaland Region
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Progesterone vaginal tablet

What is Progesterone vaginal tablet?

Progesterone vaginal tablet is a Small molecule drug developed by Vastra Gotaland Region.

Who makes Progesterone vaginal tablet?

Progesterone vaginal tablet is developed and marketed by Vastra Gotaland Region (see full Vastra Gotaland Region pipeline at /company/vastra-gotaland-region).

Is Progesterone vaginal tablet also known as anything else?

Progesterone vaginal tablet is also known as Lutinus, manufactured by Ferring GmbH. ATC code G03DA04.

What development phase is Progesterone vaginal tablet in?

Progesterone vaginal tablet is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing