NDC codes

FDA NDC Directory
Product NDC (as listed)51862-376Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51862-0376Add 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 NDC11-digit (billing)PackageCopy
51862-376-12518620376121 CAN in 1 CARTON (51862-376-12) / 120 g in 1 CANMarketed from Apr 11, 2017

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)
Sorilux
Generic name (nonproprietary)
calcipotriene
Active ingredients
Calcipotriene — 50 ug/g
Dosage form
Aerosol, Foam
Route
Topical
Labeler
Mayne PharmaNDC labeler code 51862
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 022563
Marketing start
Listing expires
Other FDA classes
Vitamin D (Chemical structure)
Identifiers
Product ID 51862-376_cf0e1842-298b-47e7-9d51-f0789ae086caSPL ID cf0e1842-298b-47e7-9d51-f0789ae086caSPL set ID 51f208d0-7b3f-44cc-8bed-92fa3d2e7bbeRxCUI 1020035, 1020039UNII 143NQ3779B
Pharmacologic class
Vitamin D Analog

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 HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451862037612 followed by a unit qualifier and the quantity

Package 51862-0376-12. 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 .

Indications (excerpt from the label)

SORILUX Foam is indicated for the topical treatment of plaque psoriasis of the scalp and body in adults and pediatric patients 4 years of age and older. SORILUX ® Foam is a vitamin D analog indicated for the topical treatment of plaque psoriasis of the scalp and body in adults and pediatric patients 4 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51862-376

What is NDC 51862-376?
51862-376 is the product NDC for Sorilux (calcipotriene), Calcipotriene 50 ug/g aerosol, foam, listed with the FDA by Mayne Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sorilux (Calcipotriene).
What is the active ingredient?
Calcipotriene.
Who is the labeler?
Mayne Pharma, NDC labeler code 51862. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sorilux?
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.

Other NDCs under NDA 022563

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 022563
ProductStrengthForm · routeLabelerProduct NDC
calcipotrieneCalcipotriene 50 ug/gAerosol, FoamTopicalMayne Pharma51862-512

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Sorilux NDC 51862-376 | National Drug Code | Med-Code