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FDA NDA · NDA018089

UTICORT

Sponsor: PARKE DAVIS

APPLICATION
NDA018089
TYPE
NDA
ROUTE
TOPICAL
DOSAGE FORM
OINTMENT
MARKETING STATUS
Discontinued

Products

UTICORTDiscontinued
BETAMETHASONE BENZOATE 0.025% · OINTMENT · TOPICAL
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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