NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1401Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1401Add 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
72162-1401-2721621401021 TUBE in 1 CARTON (72162-1401-2) / 15 g in 1 TUBEMarketed from Mar 11, 2024
72162-1401-3721621401031 TUBE in 1 CARTON (72162-1401-3) / 30 g in 1 TUBEMarketed from Mar 11, 2024
72162-1401-6721621401061 TUBE in 1 CARTON (72162-1401-6) / 60 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)
Fluticasone Propionate
Generic name (nonproprietary)
fluticasone propionate
Active ingredients
Fluticasone propionate — .05 mg/g
Dosage form
Ointment
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076668
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-1401_1e245565-3fcf-4630-bf13-326fffbce74cSPL ID 1e245565-3fcf-4630-bf13-326fffbce74cSPL set ID 8204a0c2-bd24-409a-b848-b3b369df642fRxCUI 895487UNII O2GMZ0LF5W
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

N472162140102 followed by a unit qualifier and the quantity

Package 72162-1401-02. 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)

Fluticasone propionate ointment is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in adult patients. Fluticasone propionate ointment is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in adult patients. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076668

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

FDA NDC Directory listings under ANDA 076668
ProductStrengthForm · routeLabelerProduct NDC
Fluticasone PropionateFluticasone propionate .05 mg/gOintmentTopicalBryant Ranch Prepack63629-8662
Fluticasone PropionateFluticasone propionate .05 mg/gOintmentTopicalBryant Ranch Prepack63629-8661
Fluticasone PropionateFluticasone propionate .05 mg/gOintmentTopicalBryant Ranch Prepack63629-8663
Fluticasone PropionateFluticasone propionate .05 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-221

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