NDC codes

FDA NDC Directory
Product NDC (as listed)68788-4120Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-4120Add 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
68788-4120-1687884120011 BOTTLE, SPRAY in 1 CARTON (68788-4120-1) / 120 SPRAY in 1 BOTTLE, SPRAYMarketed from Jun 8, 2026

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 — 50 ug/1
Dosage form
Spray
Route
Nasal
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218321
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68788-4120_8225d521-f1f7-4d21-9095-9a2e1833d1bfSPL ID 8225d521-f1f7-4d21-9095-9a2e1833d1bfSPL set ID 8225d521-f1f7-4d21-9095-9a2e1833d1bfRxCUI 1797907UNII 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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468788412001 followed by a unit qualifier and the quantity

Package 68788-4120-01. 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 nasal spray is indicated for the management of the nasal symptoms of perennial nonallergic rhinitis in adults and pediatric patients aged 4 years and older. Fluticasone propionate nasal spray is a corticosteroid indicated for the management of the nasal symptoms of perennial nonallergic rhinitis in adult and pediatric patients aged 4 years and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218321

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

FDA NDC Directory listings under ANDA 218321
ProductStrengthForm · routeLabelerProduct NDC
Fluticasone PropionateFluticasone propionate 50 ug/1SprayNasalNuCare Pharmaceuticals, Inc.68071-3949
Fluticasone PropionateFluticasone propionate 50 ug/1SprayNasalAdvagen Pharma Ltd72888-141

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