NDC codes

FDA NDC Directory
Product NDC (as listed)72657-159Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72657-0159Add 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
72657-159-12726570159121 BOTTLE in 1 CARTON (72657-159-12) / 120 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-14726570159141 BOTTLE in 1 CARTON (72657-159-14) / 144 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-24726570159242 BOTTLE in 1 CARTON (72657-159-24) / 120 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-28726570159282 BOTTLE in 1 CARTON (72657-159-28) / 144 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-36726570159363 BOTTLE in 1 CARTON (72657-159-36) / 120 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-42726570159423 BOTTLE in 1 CARTON (72657-159-42) / 144 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-48726570159484 BOTTLE in 1 CARTON (72657-159-48) / 120 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-60726570159601 BOTTLE in 1 CARTON (72657-159-60) / 60 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 2026
72657-159-72726570159721 BOTTLE in 1 CARTON (72657-159-72) / 72 SPRAY, METERED in 1 BOTTLEMarketed from Mar 16, 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 ALLERGY RELIEFSuffix: ALLERGY RELIEF
Generic name (nonproprietary)
fluticasone propionate
Active ingredients
Fluticasone propionate — 50 ug/1
Dosage form
Spray, Metered
Route
Nasal
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218742
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72657-159_282e11b5-3962-4e31-87c0-18163fa04f92SPL ID 282e11b5-3962-4e31-87c0-18163fa04f92SPL set ID 5494106f-6792-409e-b63f-b63b98140959RxCUI 1797907UNII O2GMZ0LF5WUPC 0372657159128
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

N472657015912 followed by a unit qualifier and the quantity

Package 72657-0159-12. 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)

Uses Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • itchy nose • runny nose • itchy, watery eyes • sneezing

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218742

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

FDA NDC Directory listings under ANDA 218742
ProductStrengthForm · routeLabelerProduct NDC
Childrens Fluticasone Propionate ALLERGY RELIEFfluticasone propionateFluticasone propionate 50 ug/1Spray, MeteredNasalGLENMARK THERAPEUTICS INC., USA72657-166
Fluticasone Propionate ALLERGY RELIEFfluticasone propionateFluticasone propionate 50 ug/1Spray, MeteredNasalYYBA CORP73581-530

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