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LUMISIGHT

NDA · New Drug Application · Sponsor: LUMICELL · Approved 2024-04-17

Drug application

FDA Application #
NDA214511
Application type
New Drug Application
Brand name
LUMISIGHT
Generic name
PEGULICIANINE
Active ingredients
PEGULICIANINE ACETATE
Dosage form
POWDER
Route
INTRAVENOUS
Marketing status
Prescription
Sponsor
LUMICELL
Manufacturer
Lumicell, Inc.
First approval
2024-04-17

Source

Authoritative
Drugs@FDA application overview
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