Prescription drug · ANDA
Fenofibrate NDC 50090-6974
Fenofibrate 160 mg/1 · Tablet · Oral · A-S Medication Solutions
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50090-6974-0 | 50090697400 | 90 TABLET in 1 BOTTLE (50090-6974-0)Marketed from Dec 21, 2023 |
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
- A-S Medication Solutions
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076509
- Marketing start
- Listing expires
- Identifiers
- Product ID 50090-6974_ceae8452-995f-4005-b8a5-b482b47ca580SPL ID ceae8452-995f-4005-b8a5-b482b47ca580SPL set ID f937a176-3d3e-4dc6-a7d4-c1a4749c7a7fRxCUI 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
N450090697400followed by a unit qualifier and the quantityPackage 50090-6974-00. 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)
Fenofibrate is a peroxisome proliferator-activated receptor (PPAR) alpha agonist indicated as an adjunct to diet: To reduce elevated LDL-C, Total-C, TG and Apo B, and to increase HDL-C in adult patients with primary hypercholesterolemia or mixed dyslipidemia. ( 1.1 ) For treatment of adult patients with severe hypertriglyceridemia. ( 1.2 ) Limitations of Use: Fenofibrate was not shown to reduce coronary heart disease morbidity and mortality in patients with type 2 diabetes mellitus. ( 5.1 ) 1.1 Primary Hypercholesterolemia or Mixed Dyslipidemia Fenofibrate tablets are indicated as adjunctive therapy to diet to reduce elevated low-density lipoprotein cholesterol (LDL-C), total cholesterol (T…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 076509
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 | Northwind Health Company, LLC | 51655-009 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4326 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-410 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 0115-5511 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 0115-5522 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | Amneal Pharmaceuticals LLC | 60219-5511 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | Amneal Pharmaceuticals LLC | 60219-5522 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | AvPAK | 50268-313 |
| Fenofibrate | Fenofibrate 54 mg/1 | TabletOral | AvPAK | 50268-312 |
| Fenofibrate | Fenofibrate 160 mg/1 | TabletOral | A-S Medication Solutions | 50090-6973 |