What is NDC 69367-242?

69367-242 is the product NDC for Nabumetone, Nabumetone 750 mg/1 tablet, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Westminster Pharmaceuticals, LLC, NDC labeler code 69367. 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 69367-242 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69367-242Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69367-0242Add 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
69367-242-01	69367024201	100 TABLET in 1 BOTTLE, PLASTIC (69367-242-01)Marketed from Sep 25, 2019
69367-242-05	69367024205	500 TABLET in 1 BOTTLE, PLASTIC (69367-242-05)Marketed from Sep 25, 2019

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 — 750 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Westminster Pharmaceuticals, LLCNDC labeler code 69367
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078420
Marketing start: Sep 25, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 69367-242_9e0fbde4-6738-44ed-964a-2de2008ca71fSPL ID 9e0fbde4-6738-44ed-964a-2de2008ca71fSPL set ID 264df44a-e294-4d9b-9113-92859cb08c20RxCUI 311892, 311893UNII LW0TIW155ZUPC 0369367242059
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

N469367024201 followed by a unit qualifier and the quantity

Package 69367-0242-01. 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

Current FDA label (SPL), effective Aug 30, 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 69367-242

What is NDC 69367-242?: 69367-242 is the product NDC for Nabumetone, Nabumetone 750 mg/1 tablet, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 2 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?: Westminster Pharmaceuticals, LLC, NDC labeler code 69367. 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	PD-Rx Pharmaceuticals, Inc.	72789-040
Nabumetone	Nabumetone 500 mg/1	TabletOral	Proficient Rx LP	71205-977
Nabumetone	Nabumetone 500 mg/1	TabletOral	direct rx	72189-184
Nabumetone	Nabumetone 750 mg/1	TabletOral	Proficient Rx LP	71205-978
Nabumetone	Nabumetone 750 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0104
Nabumetone	Nabumetone 750 mg/1	TabletOral	Bryant Ranch Prepack	71335-1559
Nabumetone	Nabumetone 750 mg/1	TabletOral	REMEDYREPACK INC.	70518-4047
Nabumetone	Nabumetone 750 mg/1	TabletOral	Northwind Health Company, LLC	51655-733
Nabumetone	Nabumetone 500 mg/1	TabletOral	Bryant Ranch Prepack	72162-1557
Nabumetone	Nabumetone 750 mg/1	TabletOral	Bryant Ranch Prepack	72162-1558
Nabumetone	Nabumetone 750 mg/1	TabletOral	A-S Medication Solutions	50090-6167
Nabumetone	Nabumetone 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-210
Nabumetone	Nabumetone 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7765
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 500 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-241
Nabumetone	Nabumetone 750 mg/1	TabletOral	Proficient Rx LP	71205-530
Nabumetone	Nabumetone 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-2292
Nabumetone	Nabumetone 500 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-368

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