NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1396Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1396Add 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
72162-1396-272162139602721621396021 TUBE in 1 CARTON (72162-1396-2) / 15 g in 1 TUBEMarketed from Mar 11, 2024
72162-1396-472162139604721621396041 TUBE in 1 CARTON (72162-1396-4) / 50 g in 1 TUBEMarketed from Mar 11, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Halobetasol Propionate
Generic name (nonproprietary)
halobetasol propionate
Active ingredients
Halobetasol propionate — .5 mg/g
Dosage form
Ointment
Route
Topical
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076872
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-1396_fcb21245-f0e9-4ffc-82bb-2667e55586afSPL ID fcb21245-f0e9-4ffc-82bb-2667e55586afSPL set ID be683823-9c07-498c-8357-71cbb3a3964cRxCUI 977978UNII 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

N472162139602 followed by a unit qualifier and the quantity

Package 72162-1396-02. 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)

INDICATIONS AND USAGE Halobetasol propionate ointment, 0.05% is a super-high potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Treatment beyond two consecutive weeks is not recommended, and the total dosage should not exceed 50 g/week because of the potential for the drug to suppress the hypothalamic-pituitary-adrenal (HPA) axis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-1396

What is NDC 72162-1396?
72162-1396 is the product NDC for Halobetasol Propionate, Halobetasol propionate .5 mg/g ointment, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Halobetasol Propionate.
What is the active ingredient?
Halobetasol propionate.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Halobetasol Propionate?
13 other product NDCs are listed under this name. See all Halobetasol Propionate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Halobetasol Propionate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalEncube Ethicals, Inc.21922-10821922-0108-0421922-0108-14
Halobetasol PropionateHalobetasol propionate .5 mg/gLotionTopicalCoral Way Pharma, LLC85437-00885437-0008-60
Halobetasol propionateHalobetasol propionate .5 mg/gAerosol, FoamTopicalMayne Pharma68308-76968308-0769-50
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalQUAGEN PHARMACEUTICALS LLC70752-11970752-0119-0270752-0119-04
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalBryant Ranch Prepack72162-206772162-2067-0272162-2067-04
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-13145802-0131-3245802-0131-35
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalBryant Ranch Prepack63629-866463629-8664-01
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalBryant Ranch Prepack63629-866563629-8665-01
Halobetasol PropionateHalobetasol propionate .5 mg/gCreamTopicalPadagis Israel Pharmaceuticals Ltd45802-12945802-0129-3245802-0129-35
Halobetasol PropionateHalobetasol propionate .5 mg/gCreamTopicalBryant Ranch Prepack72162-233172162-2331-02

All 14 Halobetasol Propionate NDCs

Other NDCs under ANDA 076872

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

FDA NDC Directory listings under ANDA 076872
ProductStrengthForm · routeLabelerProduct NDC
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-131
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalBryant Ranch Prepack63629-8664
Halobetasol PropionateHalobetasol propionate .5 mg/gOintmentTopicalBryant Ranch Prepack63629-8665

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