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FDA NDA · NDA210933

EYSUVIS

loteprednol etabonate

Sponsor: ALCON LABS INC

APPLICATION
NDA210933
TYPE
NDA
ORIGINAL APPROVAL
2020-10-26
LATEST ACTION
2020-10-26
ROUTE
OPHTHALMIC
DOSAGE FORM
SUSPENSION/DROPS
MARKETING STATUS
Prescription

Products

EYSUVIS · ReferencePrescription
LOTEPREDNOL ETABONATE 0.25% · SUSPENSION/DROPS · OPHTHALMIC

Approval history

2020-10-26Type 10 - New Indication Submitted as Distinct NDA - Not Consolidated · Original · standardLabelAP
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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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