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Mizollen (MIZOLASTINE)

Sanofi · FDA-approved approved Small molecule Quality 26/100

Mizollen (generic name: MIZOLASTINE) is a mizolastine Small molecule drug developed by Sanofi. It is currently FDA-approved (first approved 1998) for Allergic rhinitis, Perennial allergic rhinitis.

At a glance

Generic nameMIZOLASTINE
SponsorSanofi
Drug classmizolastine
TargetHistamine H1 receptor
ModalitySmall molecule
Therapeutic areaOther
PhaseFDA-approved
First approval1998

Approved indications

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
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about Mizollen

What is Mizollen?

Mizollen (MIZOLASTINE) is a mizolastine drug developed by Sanofi, indicated for Allergic rhinitis, Perennial allergic rhinitis.

What is Mizollen used for?

Mizollen is indicated for Allergic rhinitis, Perennial allergic rhinitis.

Who makes Mizollen?

Mizollen is developed and marketed by Sanofi (see full Sanofi pipeline at /company/sanofi).

What is the generic name of Mizollen?

MIZOLASTINE is the generic (nonproprietary) name of Mizollen.

What drug class is Mizollen in?

Mizollen belongs to the mizolastine class. See all mizolastine drugs at /class/mizolastine.

When was Mizollen approved?

Mizollen was first approved on 1998.

What development phase is Mizollen in?

Mizollen is FDA-approved (marketed).

What does Mizollen target?

Mizollen targets Histamine H1 receptor and is a mizolastine.

Related

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