What is NDC 68180-141?

68180-141 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, film coated, listed with the FDA by Lupin Pharmaceuticals, Inc..

Lupin Pharmaceuticals, Inc., NDC labeler code 68180. 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?

58 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 68180-141 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68180-141Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68180-0141Add the package segment from the table below.

Product information

Brand name (proprietary): Nabumetone
Generic name (nonproprietary): nabumetone
Active ingredients: Nabumetone — 500 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090445
Marketing start: Jan 12, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 68180-141_54834b73-96d1-4f73-953d-a3407be454d6SPL ID 54834b73-96d1-4f73-953d-a3407be454d6SPL set ID cf96d189-5417-4181-a5fb-169b269560a2RxCUI 311892, 311893UNII LW0TIW155ZUPC 0368180142010, 0368180141013
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.

Product label

Current FDA label (SPL), effective Nov 3, 2023. 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 USP. 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 68180-141

What is NDC 68180-141?: 68180-141 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, film coated, listed with the FDA by Lupin Pharmaceuticals, Inc..
What drug is associated with this NDC?: Nabumetone.
What is the active ingredient?: Nabumetone.
Who is the labeler?: Lupin Pharmaceuticals, Inc., NDC labeler code 68180. 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?: 58 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 59 Nabumetone NDCs

Other NDCs under ANDA 090445

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

FDA NDC Directory listings under ANDA 090445
Product	Strength	Form · route	Labeler	Product NDC
Nabumetone	Nabumetone 750 mg/1	Tablet, Film coatedOral	Lupin Pharmaceuticals, Inc.	68180-142