What is NDC 82292-040?

82292-040 is the product NDC for Lumisight (pegulicianine), Pegulicianine 10 mg/mL injection, powder, lyophilized, for solution, listed with the FDA by Lumicell, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Lumicell, Inc., NDC labeler code 82292. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lumisight?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lumisight NDC 82292-040 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82292-040Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82292-0040Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
82292-040-10	82292004010	10 VIAL in 1 CARTON (82292-040-10) / 3.9 mL in 1 VIAL (82292-040-01)Marketed from Apr 17, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Lumisight
Generic name (nonproprietary): pegulicianine
Active ingredients: Pegulicianine — 10 mg/mL
Dosage form: Injection, Powder, Lyophilized, For solution
Route: Intravenous
Labeler: Lumicell, Inc.NDC labeler code 82292
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 214511
Marketing start: Apr 17, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 82292-040_8a6aec36-4e75-4cd0-a250-cb126128bbd4SPL ID 8a6aec36-4e75-4cd0-a250-cb126128bbd4SPL set ID 7160e774-663a-43e4-ba4a-06cc57830e66UNII T6HE85WN0Q

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N482292004010 followed by a unit qualifier and the quantity

Package 82292-0040-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 9, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

LUMISIGHT is indicated for fluorescence imaging in adults with breast cancer as an adjunct for the intraoperative detection of cancerous tissue within the resection cavity following removal of the primary specimen during lumpectomy surgery. LUMISIGHT is an optical imaging agent indicated for fluorescence imaging in adults with breast cancer as an adjunct for the intraoperative detection of cancerous tissue within the resection cavity following removal of the primary specimen during lumpectomy surgery. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82292-040

What is NDC 82292-040?: 82292-040 is the product NDC for Lumisight (pegulicianine), Pegulicianine 10 mg/mL injection, powder, lyophilized, for solution, listed with the FDA by Lumicell, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lumisight (Pegulicianine).
What is the active ingredient?: Pegulicianine.
Who is the labeler?: Lumicell, Inc., NDC labeler code 82292. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lumisight?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Lumisight (Pegulicianine) NDC 82292-040