Allergy Relief (fluticasone propionate) NDC 59726-203

Product information

Brand name (proprietary)

Allergy Relief

Generic name (nonproprietary)

fluticasone propionate

Active ingredients

Fluticasone propionate — 50 ug/1

Dosage form

Spray, Metered

Route

Nasal

Labeler

P & L Development, LLC

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208150

Marketing start

May 15, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Corticosteroid Hormone Receptor Agonists (Mechanism)

Identifiers

Product ID 59726-203_c180ed31-17af-48cf-a484-dc1e96911704SPL ID c180ed31-17af-48cf-a484-dc1e96911704SPL set ID f83fabaa-1c6c-4a19-9f30-2f06df6d48f4RxCUI 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

N459726020338 followed by a unit qualifier and the quantity Copy

Package 59726-0203-38. 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

Other NDCs under ANDA 208150

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