Prescription drug · ANDA
Fenofibrate NDC 71335-1756
Fenofibrate 160 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-1756-1 | 71335175601 | 30 TABLET in 1 BOTTLE (71335-1756-1)Marketed from Dec 20, 2021 | |
| 71335-1756-2 | 71335175602 | 90 TABLET in 1 BOTTLE (71335-1756-2)Marketed from Dec 20, 2021 | |
| 71335-1756-3 | 71335175603 | 60 TABLET in 1 BOTTLE (71335-1756-3)Marketed from Dec 20, 2021 | |
| 71335-1756-4 | 71335175604 | 28 TABLET in 1 BOTTLE (71335-1756-4)Marketed from Dec 20, 2021 | |
| 71335-1756-5 | 71335175605 | 100 TABLET in 1 BOTTLE (71335-1756-5)Marketed from Dec 20, 2021 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Fenofibrate
- Generic name (nonproprietary)
- fenofibrate
- Active ingredients
- Fenofibrate — 160 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213864
- Marketing start
- Listing expires
- Identifiers
- Product ID 71335-1756_e4d10350-019b-430a-a9c7-0719b1bc65b6SPL ID e4d10350-019b-430a-a9c7-0719b1bc65b6SPL set ID d34f9fa3-39ae-4b8e-8f29-0d5c655c50b5RxCUI 349287UNII U202363UOS
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471335175601followed by a unit qualifier and the quantityPackage 71335-1756-01. 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.
Other NDCs under ANDA 213864
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 |
|---|---|---|---|---|
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | A-S Medication Solutions | 50090-7926 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | A-S Medication Solutions | 50090-7927 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | Lifestar Pharma LLC | 70756-214 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | Proficient Rx LP | 71205-666 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | Lifestar Pharma LLC | 70756-215 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | Major Pharmaceuticals | 0904-7539 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-318 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-7816 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-856 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | NorthStar RxLLC | 72603-841 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | NorthStar RxLLC | 72603-840 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2907 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2947 |