# LUMISIGHT

NDC: 82292-040
Generic name: Pegulicianine
Labeler / Manufacturer: Lumicell, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240417

FDA application: NDA214511

## Active ingredients

- PEGULICIANINE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82292-040"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82292-040
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7160e774-663a-43e4-ba4a-06cc57830e66