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Sublingual Misoprostol

Stony Brook University · FDA-approved active Small molecule ✓ Verified May 2026 Quality 5/100

Sublingual Misoprostol is a Small molecule drug developed by Stony Brook University. It is currently FDA-approved. Also known as: experimental, two tablets of Cytotec (200 μg), cytotec, Prostokos.

Sublingual misoprostol is a small molecule used to treat various conditions, including bleeding during myomectomy, miscarriage, labor onset and length abnormalities, missed miscarriage, and incomplete abortion. It is administered sublingually, a method of administration where the medication is placed under the tongue.

At a glance

Generic nameSublingual Misoprostol
Also known asexperimental, two tablets of Cytotec (200 μg), cytotec, Prostokos, Cytotec
SponsorStony Brook University
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 Sublingual Misoprostol

What is Sublingual Misoprostol?

Sublingual Misoprostol is a Small molecule drug developed by Stony Brook University.

Who makes Sublingual Misoprostol?

Sublingual Misoprostol is developed and marketed by Stony Brook University (see full Stony Brook University pipeline at /company/stony-brook-university).

Is Sublingual Misoprostol also known as anything else?

Sublingual Misoprostol is also known as experimental, two tablets of Cytotec (200 μg), cytotec, Prostokos, Cytotec.

What development phase is Sublingual Misoprostol in?

Sublingual Misoprostol is FDA-approved (marketed).

Related

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