What is NDC 76282-257?

76282-257 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, film coated, listed with the FDA by Exelan Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Exelan Pharmaceuticals Inc., NDC labeler code 76282. 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 76282-257 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)76282-257Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76282-0257Add 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
76282-257-01	7628202570176282025701	100 TABLET, FILM COATED in 1 BOTTLE (76282-257-01)Marketed from Apr 14, 2015
76282-257-05	7628202570576282025705	500 TABLET, FILM COATED in 1 BOTTLE (76282-257-05)Marketed from Apr 14, 2015

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, Film coated
Route: Oral
Labeler: Exelan Pharmaceuticals Inc.NDC labeler code 76282
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078671
Marketing start: Apr 14, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 76282-257_11f0008a-dff5-4fd3-8f48-76d033ea87f5SPL ID 11f0008a-dff5-4fd3-8f48-76d033ea87f5SPL set ID 16e76e29-9315-40c0-b1d6-8d91961063cfRxCUI 311892, 311893UNII LW0TIW155ZUPC 0376282257013, 0376282258010
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

N476282025701 followed by a unit qualifier and the quantity

Package 76282-0257-01. 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 Mar 19, 2025. 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 76282-257

What is NDC 76282-257?: 76282-257 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, film coated, listed with the FDA by Exelan Pharmaceuticals Inc.. 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?: Exelan Pharmaceuticals Inc., NDC labeler code 76282. 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	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 58 Nabumetone NDCs

Other NDCs under ANDA 078671

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

FDA NDC Directory listings under ANDA 078671
Product	Strength	Form · route	Labeler	Product NDC
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-972
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-396
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-630
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	Cipla USA Inc.	69097-965
Nabumetone	Nabumetone 750 mg/1	Tablet, Film coatedOral	Cipla USA Inc.	69097-966
Nabumetone	Nabumetone 750 mg/1	Tablet, Film coatedOral	Exelan Pharmaceuticals Inc.	76282-258
Nabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0053