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Gaviscon (ALGELDRATE)

Sanofi · FDA-approved active Small molecule Quality 22/100

Gaviscon (generic name: ALGELDRATE) is a algeldrate Small molecule drug developed by Sanofi. It is currently FDA-approved (first approved 1983) for Duodenal ulcer disease, Gastric Hypersecretory Conditions, Gastric ulcer.

At a glance

Generic nameALGELDRATE
SponsorSanofi
Drug classalgeldrate
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1983

Approved indications

Common side effects

No common side effects on file.

Drug interactions

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 Gaviscon

What is Gaviscon?

Gaviscon (ALGELDRATE) is a algeldrate drug developed by Sanofi, indicated for Duodenal ulcer disease, Gastric Hypersecretory Conditions, Gastric ulcer.

What is Gaviscon used for?

Gaviscon is indicated for Duodenal ulcer disease, Gastric Hypersecretory Conditions, Gastric ulcer, Gastroesophageal reflux disease, Heartburn.

Who makes Gaviscon?

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

What is the generic name of Gaviscon?

ALGELDRATE is the generic (nonproprietary) name of Gaviscon.

What drug class is Gaviscon in?

Gaviscon belongs to the algeldrate class. See all algeldrate drugs at /class/algeldrate.

When was Gaviscon approved?

Gaviscon was first approved on 1983.

What development phase is Gaviscon in?

Gaviscon is FDA-approved (marketed).

Related

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