NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2137Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2137Add 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 NDC11-digit (billing)PackageCopy
67296-2137-3672962137036729621370330 TABLET in 1 BOTTLE (67296-2137-3)Marketed from Jun 26, 2019

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 — 500 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Redpharm DrugNDC labeler code 67296
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078420
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 67296-2137_46acaa7e-b06b-ae3a-e063-6394a90ac9f5SPL ID 46acaa7e-b06b-ae3a-e063-6394a90ac9f5SPL set ID 3745775e-e11a-01db-e063-6294a90a9b52RxCUI 311892UNII LW0TIW155ZUPC 0350228466011, 0350228466059, 0350228465014

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

N467296213703 followed by a unit qualifier and the quantity

Package 67296-2137-03. 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 . 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 67296-2137

What is NDC 67296-2137?
67296-2137 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, listed with the FDA by Redpharm Drug. It has 1 package NDC, 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?
Redpharm Drug, NDC labeler code 67296. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NabumetoneNabumetone 500 mg/1Tablet, Film coatedOralANI Pharmaceuticals, Inc.70954-78470954-0784-1070954-0784-20
NabumetoneNabumetone 750 mg/1Tablet, Film coatedOralANI Pharmaceuticals, Inc.70954-78570954-0785-1070954-0785-20
NabumetoneNabumetone 750 mg/1TabletOralREMEDYREPACK INC.70518-404770518-4047-0070518-4047-0170518-4047-02
NabumetoneNabumetone 500 mg/1TabletOralREMEDYREPACK INC.70518-383570518-3835-0070518-3835-01
NabumetoneNabumetone 500 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-63060687-0630-21
NabumetoneNabumetone 750 mg/1TabletOralNorthwind Health Company, LLC51655-73351655-0733-52
NabumetoneNabumetone 500 mg/1TabletOraldirect rx72189-18472189-0184-1472189-0184-3072189-0184-60+1 more
NabumetoneNabumetone 500 mg/1TabletOralNorthwind Health Company, LLC51655-44651655-0446-2051655-0446-2551655-0446-52+1 more
NabumetoneNabumetone 500 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-776568788-7765-0168788-7765-0268788-7765-03+3 more
NabumetoneNabumetone 500 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-39651655-0396-25

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
ProductStrengthForm · routeLabelerProduct NDC
NabumetoneNabumetone 500 mg/1TabletOralA-S Medication Solutions50090-5294
NabumetoneNabumetone 750 mg/1TabletOralA-S Medication Solutions50090-6167
NabumetoneNabumetone 500 mg/1TabletOralScieGen Pharmaceuticals Inc50228-465
NabumetoneNabumetone 750 mg/1TabletOralScieGen Pharmaceuticals Inc50228-466
NabumetoneNabumetone 500 mg/1TabletOralNorthwind Health Company, LLC51655-446
NabumetoneNabumetone 750 mg/1TabletOralNorthwind Health Company, LLC51655-733
NabumetoneNabumetone 750 mg/1TabletOralQuality Care Products, LLC55700-840
NabumetoneNabumetone 500 mg/1TabletOralQuality Care Products, LLC55700-845
NabumetoneNabumetone 500 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-368
NabumetoneNabumetone 750 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-369
NabumetoneNabumetone 500 mg/1TabletOralBryant Ranch Prepack63629-8506
NabumetoneNabumetone 500 mg/1TabletOralBryant Ranch Prepack63629-8508
NabumetoneNabumetone 750 mg/1TabletOralBryant Ranch Prepack63629-8509
NabumetoneNabumetone 750 mg/1TabletOralBryant Ranch Prepack63629-8510
NabumetoneNabumetone 750 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7597
NabumetoneNabumetone 500 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7765
NabumetoneNabumetone 500 mg/1TabletOralWestminster Pharmaceuticals, LLC69367-241
NabumetoneNabumetone 750 mg/1TabletOralWestminster Pharmaceuticals, LLC69367-242
NabumetoneNabumetone 500 mg/1TabletOralREMEDYREPACK INC.70518-3835
NabumetoneNabumetone 750 mg/1TabletOralREMEDYREPACK INC.70518-4047

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