Prescription drug · ANDA
Fluticasone Propionate NDC 72888-141
Fluticasone propionate 50 ug/1 · Spray · Nasal · Advagen Pharma Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72888-141-35 | 72888014135 | 1 BOTTLE, SPRAY in 1 CARTON (72888-141-35) / 120 SPRAY in 1 BOTTLE, SPRAYMarketed from Jun 5, 2025 |
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
- Route
- Nasal
- Labeler
- Advagen Pharma Ltd
- 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 72888-141_49fdadf9-f6ac-1fc3-e063-6294a90a2c09SPL ID 49fdadf9-f6ac-1fc3-e063-6294a90a2c09SPL set ID 2c1c465c-d008-470e-aa48-8b44bd60751cRxCUI 1797907UNII O2GMZ0LF5WUPC 0372888141350
- 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
N472888014135followed by a unit qualifier and the quantityPackage 72888-0141-35. 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.
Other NDCs under ANDA 218321
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Fluticasone Propionate | Fluticasone propionate 50 ug/1 | SprayNasal | NuCare Pharmaceuticals, Inc. | 68071-3949 |
| Fluticasone Propionate | Fluticasone propionate 50 ug/1 | SprayNasal | Preferred Pharmaceuticals Inc. | 68788-4120 |