What is NDC 72189-184?

72189-184 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, listed with the FDA by direct rx. It has 4 package NDCs, shown above in 10- and 11-digit form.

direct rx, NDC labeler code 72189. 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?

57 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 72189-184 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-184Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0184Add 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
72189-184-14	7218901841472189018414	14 TABLET in 1 BOTTLE (72189-184-14)Marketed from May 11, 2021
72189-184-30	7218901843072189018430	30 TABLET in 1 BOTTLE (72189-184-30)Marketed from May 11, 2021
72189-184-60	7218901846072189018460	60 TABLET in 1 BOTTLE (72189-184-60)Marketed from May 11, 2021
72189-184-90	7218901849072189018490	90 TABLET in 1 BOTTLE (72189-184-90)Marketed from May 11, 2021

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): Nabumetone
Generic name (nonproprietary): nabumetone
Active ingredients: Nabumetone — 500 mg/1
Dosage form: Tablet
Route: Oral
Labeler: direct rxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078420
Marketing start: May 11, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 72189-184_2be95f19-e557-ab96-e063-6394a90a6947SPL ID 2be95f19-e557-ab96-e063-6394a90a6947SPL set ID a8600b12-f180-0b27-e053-2995a90acbd9RxCUI 311892, 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

N472189018414 followed by a unit qualifier and the quantity

Package 72189-0184-14. 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 Jan 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Carefully consider the potential benefits and risks of nabumetone tablets 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 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 72189-184

What is NDC 72189-184?: 72189-184 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, listed with the FDA by direct rx. 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?: direct rx, NDC labeler code 72189. 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?: 57 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	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
Nabumetone	Nabumetone 750 mg/1	TabletOral	direct rx	72189-072	72189-0072-1472189-0072-3072189-0072-60

All 58 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 500 mg/1	TabletOral	A-S Medication Solutions	50090-5294
Nabumetone	Nabumetone 750 mg/1	TabletOral	A-S Medication Solutions	50090-6167
Nabumetone	Nabumetone 500 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-465
Nabumetone	Nabumetone 750 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-466
Nabumetone	Nabumetone 500 mg/1	TabletOral	Northwind Health Company, LLC	51655-446
Nabumetone	Nabumetone 750 mg/1	TabletOral	Northwind Health Company, LLC	51655-733
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	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	63629-8506
Nabumetone	Nabumetone 500 mg/1	TabletOral	Bryant Ranch Prepack	63629-8508
Nabumetone	Nabumetone 750 mg/1	TabletOral	Bryant Ranch Prepack	63629-8509
Nabumetone	Nabumetone 750 mg/1	TabletOral	Bryant Ranch Prepack	63629-8510
Nabumetone	Nabumetone 500 mg/1	TabletOral	Redpharm Drug	67296-2137
Nabumetone	Nabumetone 750 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7597
Nabumetone	Nabumetone 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7765
Nabumetone	Nabumetone 500 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-241
Nabumetone	Nabumetone 750 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-242
Nabumetone	Nabumetone 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-3835

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