NDC codes

FDA NDC Directory
Product NDC (as listed)51407-871Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51407-0871Add 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
51407-871-12514070871121 BOTTLE, GLASS in 1 CARTON (51407-871-12) / 120 SPRAY, METERED in 1 BOTTLE, GLASSMarketed from Mar 10, 2026

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)
Fluticasone Propionate
Generic name (nonproprietary)
fluticasone propionate
Active ingredients
Fluticasone propionate — 50 ug/1
Dosage form
Spray, Metered
Route
Nasal
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076504
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 51407-871_5852b1a7-401d-e06b-e063-6294a90a2530SPL ID 5852b1a7-401d-e06b-e063-6294a90a2530SPL set ID 534d78c5-4ba0-4ab1-e063-6294a90a8ff7RxCUI 1797907UNII O2GMZ0LF5WUPC 0351407871121
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

N451407087112 followed by a unit qualifier and the quantity

Package 51407-0871-12. 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 076504

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

FDA NDC Directory listings under ANDA 076504
ProductStrengthForm · routeLabelerProduct NDC
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalPreferred Pharmaceuticals Inc.68788-8446
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalA-S Medication Solutions50090-2880
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalHikma Pharmaceuticals USA Inc.0054-3270
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalREMEDYREPACK INC.70518-0880
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalAsclemed USA, Inc.76420-329
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalProficient Rx LP63187-806
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalNuCare Pharmaceuticals,Inc.68071-4868

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