What is NDC 50090-6167?

50090-6167 is the product NDC for Nabumetone, Nabumetone 750 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 4 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 Nabumetone?

59 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Nabumetone NDC 50090-6167 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-6167Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-6167Add 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
50090-6167-0	50090616700	30 TABLET in 1 BOTTLE (50090-6167-0)Marketed from Oct 13, 2022
50090-6167-2	50090616702	14 TABLET in 1 BOTTLE (50090-6167-2)Marketed from Oct 13, 2022
50090-6167-3	50090616703	60 TABLET in 1 BOTTLE (50090-6167-3)Marketed from Oct 13, 2022
50090-6167-4	50090616704	20 TABLET in 1 BOTTLE (50090-6167-4)Marketed from Oct 13, 2022

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): Nabumetone
Generic name (nonproprietary): nabumetone
Active ingredients: Nabumetone — 750 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 078420
Marketing start: Jun 26, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 50090-6167_ae902cbe-e8b4-42c9-8e85-828d7ca2d2f6SPL ID ae902cbe-e8b4-42c9-8e85-828d7ca2d2f6SPL set ID d997d125-dfc5-4cc5-b7a6-03f5a7248d14RxCUI 311893UNII LW0TIW155Z
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N450090616700 followed by a unit qualifier and the quantity

Package 50090-6167-00. 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 Oct 25, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of nabumetone tablets, USP and other treatment options before deciding to use nabumetone tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Nabumetone tablets, USP are indicated for relief of signs and symptoms of osteoarthritis and rheumatoid arthritis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-6167

What is NDC 50090-6167?: 50090-6167 is the product NDC for Nabumetone, Nabumetone 750 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nabumetone.
What is the active ingredient?: Nabumetone.
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 Nabumetone?: 59 other product NDCs are listed under this name. See all Nabumetone 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 Nabumetone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	ANI Pharmaceuticals, Inc.	70954-784	70954-0784-1070954-0784-20
Nabumetone	Nabumetone 750 mg/1	Tablet, Film coatedOral	ANI Pharmaceuticals, Inc.	70954-785	70954-0785-1070954-0785-20
Nabumetone	Nabumetone 750 mg/1	TabletOral	REMEDYREPACK INC.	70518-4047	70518-4047-0070518-4047-0170518-4047-02
Nabumetone	Nabumetone 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-3835	70518-3835-0070518-3835-01
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-630	60687-0630-21
Nabumetone	Nabumetone 750 mg/1	TabletOral	Northwind Health Company, LLC	51655-733	51655-0733-52
Nabumetone	Nabumetone 500 mg/1	TabletOral	direct rx	72189-184	72189-0184-1472189-0184-3072189-0184-60+1 more
Nabumetone	Nabumetone 500 mg/1	TabletOral	Northwind Health Company, LLC	51655-446	51655-0446-2051655-0446-2551655-0446-52+1 more
Nabumetone	Nabumetone 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7765	68788-7765-0168788-7765-0268788-7765-03+3 more
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-396	51655-0396-25

All 60 Nabumetone NDCs

Other NDCs under ANDA 078420

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

FDA NDC Directory listings under ANDA 078420
Product	Strength	Form · route	Labeler	Product NDC
Nabumetone	Nabumetone 750 mg/1	TabletOral	Bryant Ranch Prepack	72162-1558
Nabumetone	Nabumetone 500 mg/1	TabletOral	Bryant Ranch Prepack	72162-1557
Nabumetone	Nabumetone 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7765
Nabumetone	Nabumetone 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-210
Nabumetone	Nabumetone 500 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-465
Nabumetone	Nabumetone 750 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-466
Nabumetone	Nabumetone 750 mg/1	TabletOral	ASCLEMED USA INC.	87063-292
Nabumetone	Nabumetone 750 mg/1	TabletOral	Proficient Rx LP	71205-530
Nabumetone	Nabumetone 500 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-368
Nabumetone	Nabumetone 750 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-369
Nabumetone	Nabumetone 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-2292
Nabumetone	Nabumetone 750 mg/1	TabletOral	Bryant Ranch Prepack	71335-2293
Nabumetone	Nabumetone 750 mg/1	TabletOral	Quality Care Products, LLC	55700-840
Nabumetone	Nabumetone 500 mg/1	TabletOral	Quality Care Products, LLC	55700-845
Nabumetone	Nabumetone 500 mg/1	TabletOral	Northwind Health Company, LLC	51655-446
Nabumetone	Nabumetone 500 mg/1	TabletOral	Sportpharm LLC	85766-261
Nabumetone	Nabumetone 750 mg/1	TabletOral	Sportpharm LLC	85766-262
Nabumetone	Nabumetone 500 mg/1	TabletOral	A-S Medication Solutions	50090-5294
Nabumetone	Nabumetone 750 mg/1	TabletOral	direct rx	72189-072
Nabumetone	Nabumetone 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-1391

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