Prescription drug · ANDA
Flunisolide NDC 50742-317
Flunisolide .25 mg/mL · Solution · Nasal · Ingenus Pharmaceuticals, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50742-317-25 | 50742031725 | 1 BOTTLE, PUMP in 1 CARTON (50742-317-25) / 25 mL in 1 BOTTLE, PUMPMarketed from Jun 23, 2022 |
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)
- Flunisolide
- Generic name (nonproprietary)
- flunisolide
- Active ingredients
- Flunisolide — .25 mg/mL
- Dosage form
- Solution
- Route
- Nasal
- Labeler
- Ingenus Pharmaceuticals, LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 207802
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 50742-317_139fb92c-bb10-4ee9-8572-679ac540aa27SPL ID 139fb92c-bb10-4ee9-8572-679ac540aa27SPL set ID f39cae46-c68f-47ef-82f3-4fd3dd46c74cRxCUI 1797863UNII QK4DYS664X
- 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
N450742031725followed by a unit qualifier and the quantityPackage 50742-0317-25. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.