Is Lumicell, Inc. FDA approved?

Lumicell, Inc. holds no registered establishment of its own; 1 drug product is listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does Lumicell, Inc. make?

1 product is listed under Lumicell, Inc. in the openFDA NDC Directory, most often as injection, powder, lyophilized, for solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Lumicell, Inc.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 0
Active NDC listings: 1
Live patents: 6
Exclusivities: 1
Countries: 0

Exclusivity

Patents and exclusivities

Patent	Product	Covers	Expiry
11592396	LUMISIGHTpegulicianine acetate	substance	Sept 2030
9155471	LUMISIGHTpegulicianine acetate	use	Oct 2031
10285759	LUMISIGHTpegulicianine acetate	use	Dec 2031
9032965	LUMISIGHTpegulicianine acetate	use	Dec 2031
9532835	LUMISIGHTpegulicianine acetate	use	Dec 2031
9763577	LUMISIGHTpegulicianine acetate	substance, product	Sept 2034

Product	Exclusivity	Until
LUMISIGHTPEGULICIANINE ACETATE	NCE New chemical entity	Apr 2029

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
LUMISIGHT	Pegulicianine	injection, powder, lyophilized, for solution, intravenous	82292-040NDA

Enquiry

Common questions

Is Lumicell, Inc. FDA approved?: Lumicell, Inc. holds no registered establishment of its own; 1 drug product is listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Lumicell, Inc. make?: 1 product is listed under Lumicell, Inc. in the openFDA NDC Directory, most often as injection, powder, lyophilized, for solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.