What is NDC 51862-618?

51862-618 is the product NDC for Lexette (halobetasol propionate), Halobetasol propionate .5 mg/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?

Lexette (Halobetasol propionate).

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 Lexette?

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.

Lexette NDC 51862-618 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51862-618Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51862-0618Add 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
51862-618-50	51862061850	1 CANISTER in 1 CARTON (51862-618-50) / 50 g in 1 CANISTERMarketed from Aug 8, 2025

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): Lexette
Generic name (nonproprietary): halobetasol propionate
Active ingredients: Halobetasol propionate — .5 mg/g
Dosage form: Aerosol, Foam
Route: Topical
Labeler: Mayne PharmaNDC labeler code 51862
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215266
Marketing start: Aug 8, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51862-618_8aa1f819-c81f-4af1-aaa7-353df3203ff6SPL ID 8aa1f819-c81f-4af1-aaa7-353df3203ff6SPL set ID 8aa1f819-c81f-4af1-aaa7-353df3203ff6RxCUI 2047646, 2106585UNII 91A0K1TY3Z
Pharmacologic class: Corticosteroid

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

N451862061850 followed by a unit qualifier and the quantity

Package 51862-0618-50. 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 May 31, 2025.

Indications (excerpt from the label)

LEXETTE ® is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older. LEXETTE is a corticosteroid indicated for the topical treatment of plaque psoriasis in patients twelve (12) 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 51862-618

What is NDC 51862-618?: 51862-618 is the product NDC for Lexette (halobetasol propionate), Halobetasol propionate .5 mg/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?: Lexette (Halobetasol propionate).
What is the active ingredient?: Halobetasol propionate.
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 Lexette?: 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 ANDA 215266

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

FDA NDC Directory listings under ANDA 215266
Product	Strength	Form · route	Labeler	Product NDC
Halobetasol propionate	Halobetasol propionate .5 mg/g	Aerosol, FoamTopical	Mayne Pharma	68308-769

Lexette (Halobetasol propionate) NDC 51862-618