What is NDC 50090-7926?

50090-7926 is the product NDC for Fenofibrate, Fenofibrate 160 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 2 package NDCs, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Fenofibrate?

201 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fenofibrate NDC 50090-7926 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-7926Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-7926Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
50090-7926-0	5009079260050090792600	30 TABLET in 1 BOTTLE (50090-7926-0)Marketed from Mar 5, 2026
50090-7926-1	5009079260150090792601	90 TABLET in 1 BOTTLE (50090-7926-1)Marketed from Mar 5, 2026

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 SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213864
Marketing start: Sep 29, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 50090-7926_498e266a-53de-4d6d-bb8e-8fa2db52a449SPL ID 498e266a-53de-4d6d-bb8e-8fa2db52a449SPL set ID f443dd79-46da-4b02-8188-7417d39cf975RxCUI 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

N450090792600 followed by a unit qualifier and the quantity

Package 50090-7926-00. 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 Mar 10, 2026.

Indications (excerpt from the label)

Fenofibrate is 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 (Tota…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-7926

What is NDC 50090-7926?: 50090-7926 is the product NDC for Fenofibrate, Fenofibrate 160 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fenofibrate.
What is the active ingredient?: Fenofibrate.
Who is the labeler?: A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fenofibrate?: 201 other product NDCs are listed under this name. See all Fenofibrate NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Fenofibrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Fenofibrate	Fenofibrate 54 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4721	70518-4721-00
Fenofibrate	Fenofibrate 145 mg/1	TabletOral	REMEDYREPACK INC.	70518-4672	70518-4672-00
Fenofibrate	Fenofibrate 48 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-039	48433-0039-20
Fenofibrate	Fenofibrate 145 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-040	48433-0040-20
Fenofibrate	Fenofibrate 54 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-347	33342-0347-1033342-0347-1233342-0347-47
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-348	33342-0348-1033342-0348-1233342-0348-15
Fenofibrate	Fenofibrate 48 mg/1	TabletOral	AvKARE	73190-015	73190-0015-90
Fenofibrate	Fenofibrate 145 mg/1	TabletOral	AvKARE	73190-016	73190-0016-90
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	A-S Medication Solutions	50090-7927	50090-7927-00
Fenofibrate	Fenofibrate 54 mg/1	TabletOral	NorthStar RxLLC	72603-840	72603-0840-01

All 202 Fenofibrate NDCs

Other NDCs under ANDA 213864

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

FDA NDC Directory listings under ANDA 213864
Product	Strength	Form · route	Labeler	Product NDC
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	Major Pharmaceuticals	0904-7539
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	A-S Medication Solutions	50090-7927
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	Northwind Health Company, LLC	51655-856
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	REMEDYREPACK INC.	70518-2907
Fenofibrate	Fenofibrate 54 mg/1	TabletOral	REMEDYREPACK INC.	70518-2947
Fenofibrate	Fenofibrate 54 mg/1	TabletOral	Lifestar Pharma LLC	70756-214
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	Lifestar Pharma LLC	70756-215
Fenofibrate	Fenofibrate 54 mg/1	TabletOral	Proficient Rx LP	71205-666
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	Bryant Ranch Prepack	71335-1756
Fenofibrate	Fenofibrate 54 mg/1	TabletOral	NorthStar RxLLC	72603-840
Fenofibrate	Fenofibrate 160 mg/1	TabletOral	NorthStar RxLLC	72603-841