NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1402Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1402Add 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
72162-1402-2721621402021 TUBE in 1 CARTON (72162-1402-2) / 15 g in 1 TUBEMarketed from Aug 17, 2023
72162-1402-3721621402031 TUBE in 1 CARTON (72162-1402-3) / 30 g in 1 TUBEMarketed from Aug 17, 2023
72162-1402-6721621402061 TUBE in 1 CARTON (72162-1402-6) / 60 g in 1 TUBEMarketed from Aug 17, 2023

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 — .5 mg/g
Dosage form
Cream
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076793
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-1402_9143a0dc-a3c7-4541-9312-91e4ebacc552SPL ID 9143a0dc-a3c7-4541-9312-91e4ebacc552SPL set ID 0cd0b88c-1ab3-4699-8eda-554054b8d33cRxCUI 895987UNII 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

N472162140202 followed by a unit qualifier and the quantity

Package 72162-1402-02. 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 Fluticasone Propionate Cream, 0.05% is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Fluticasone Propionate Cream, 0.05% may be used with caution in pediatric patients 3 months of age or older. The safety and efficacy of drug use for longer than 4 weeks in this population have not been established. The safety and efficacy of Fluticasone Propionate Cream, 0.05% in pediatric patients below 3 months of age have not been established.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076793

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

FDA NDC Directory listings under ANDA 076793
ProductStrengthForm · routeLabelerProduct NDC
Fluticasone PropionateFluticasone propionate .5 mg/gCreamTopicalBryant Ranch Prepack63629-8658
Fluticasone PropionateFluticasone propionate .5 mg/gCreamTopicalBryant Ranch Prepack63629-8659
Fluticasone PropionateFluticasone propionate .5 mg/gCreamTopicalBryant Ranch Prepack63629-8660
Fluticasone PropionateFluticasone propionate .5 mg/gCreamTopicalPadagis Israel Pharmaceuticals Ltd45802-222
Fluticasone PropionateFluticasone propionate .5 mg/gCreamTopicalA-S Medication Solutions50090-1187

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