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DEXBROMPHENIRAMINE MALEATE

FDA-approved approved Small molecule Quality 15/100

DEXBROMPHENIRAMINE MALEATE is a drug. It is currently FDA-approved (first approved 1963) for Hay Fever Symptoms Relief, Upper Respiratory Allergies Symptoms Relief.

Dexbrompheniramine Maleate is a marketed antihistamine primarily indicated for the relief of hay fever symptoms. The drug's key composition patent is set to expire in 2028, providing a period of market exclusivity and potential revenue stability. The primary risk is the loss of patent protection in 2028, which could lead to increased competition from generic alternatives.

At a glance

Generic nameDEXBROMPHENIRAMINE MALEATE
ModalitySmall molecule
PhaseFDA-approved
First approval1963

Approved indications

Common side effects

No common side effects on file.

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

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Frequently asked questions about DEXBROMPHENIRAMINE MALEATE

What is DEXBROMPHENIRAMINE MALEATE?

DEXBROMPHENIRAMINE MALEATE is a Small molecule drug, indicated for Hay Fever Symptoms Relief, Upper Respiratory Allergies Symptoms Relief.

What is DEXBROMPHENIRAMINE MALEATE used for?

DEXBROMPHENIRAMINE MALEATE is indicated for Hay Fever Symptoms Relief, Upper Respiratory Allergies Symptoms Relief.

When was DEXBROMPHENIRAMINE MALEATE approved?

DEXBROMPHENIRAMINE MALEATE was first approved on 1963.

What development phase is DEXBROMPHENIRAMINE MALEATE in?

DEXBROMPHENIRAMINE MALEATE is FDA-approved (marketed).

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