← FDA Drug Approvals (Drugs@FDA)
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
- Machine
- JSON-LD · Markdown