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Besifloxacin 0.6% ophthalmic suspension

Johns Hopkins University · FDA-approved active Small molecule Quality 2/100

Besifloxacin 0.6% ophthalmic suspension is a Small molecule drug developed by Johns Hopkins University. It is currently FDA-approved. Also known as: Besivance.

At a glance

Generic nameBesifloxacin 0.6% ophthalmic suspension
Also known asBesivance
SponsorJohns Hopkins 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 Besifloxacin 0.6% ophthalmic suspension

What is Besifloxacin 0.6% ophthalmic suspension?

Besifloxacin 0.6% ophthalmic suspension is a Small molecule drug developed by Johns Hopkins University.

Who makes Besifloxacin 0.6% ophthalmic suspension?

Besifloxacin 0.6% ophthalmic suspension is developed and marketed by Johns Hopkins University (see full Johns Hopkins University pipeline at /company/johns-hopkins-university).

Is Besifloxacin 0.6% ophthalmic suspension also known as anything else?

Besifloxacin 0.6% ophthalmic suspension is also known as Besivance.

What development phase is Besifloxacin 0.6% ophthalmic suspension in?

Besifloxacin 0.6% ophthalmic suspension is FDA-approved (marketed).

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