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FDA NDA · NDA021023

RESTASIS

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APPLICATION
NDA021023
TYPE
NDA
ORIGINAL APPROVAL
2003-10-10
LATEST ACTION
2003-10-10
ROUTE
OPHTHALMIC
DOSAGE FORM
EMULSION
MARKETING STATUS
Prescription

Products

RESTASISPrescription
CYCLOSPORINE 0.05% · EMULSION · OPHTHALMIC

Approval history

2003-10-10Type 3 - New Dosage Form · Original · priorityReviewAP
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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