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Carafate

Forest Labs Inc · FDA-approved active Small molecule Quality 38/100

Carafate is a Aluminum Complex [EPC] Small molecule drug developed by Forest Labs Inc. It is currently FDA-approved (first approved 1981) for Duodenal ulcer disease, Maintenance of Healing Duodenal Ulcer.

At a glance

Generic nameCarafate
SponsorForest Labs Inc
Drug classAluminum Complex [EPC]
TargetPepsin A-5
ModalitySmall molecule
Therapeutic areaPain
PhaseFDA-approved
First approval1981

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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

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Frequently asked questions about Carafate

What is Carafate?

Carafate is a Aluminum Complex [EPC] drug developed by Forest Labs Inc, indicated for Duodenal ulcer disease, Maintenance of Healing Duodenal Ulcer.

What is Carafate used for?

Carafate is indicated for Duodenal ulcer disease, Maintenance of Healing Duodenal Ulcer.

Who makes Carafate?

Carafate is developed and marketed by Forest Labs Inc (see full Forest Labs Inc pipeline at /company/forest-labs-inc).

What drug class is Carafate in?

Carafate belongs to the Aluminum Complex [EPC] class. See all Aluminum Complex [EPC] drugs at /class/aluminum-complex-epc.

When was Carafate approved?

Carafate was first approved on 1981.

What development phase is Carafate in?

Carafate is FDA-approved (marketed).

What are the side effects of Carafate?

Common side effects of Carafate include Constipation.

What does Carafate target?

Carafate targets Pepsin A-5 and is a Aluminum Complex [EPC].

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