NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0054Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0054Add 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
80425-0054-18042500540160 TABLET in 1 BOTTLE (80425-0054-1)Marketed from Jun 26, 2019
80425-0054-28042500540290 TABLET in 1 BOTTLE (80425-0054-2)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
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 80425-0054_2a98f01a-8d9d-0770-e063-6294a90a7babSPL ID 2a98f01a-8d9d-0770-e063-6294a90a7babSPL set ID af9994ac-6687-2df2-e053-2995a90a959aRxCUI 311892UNII LW0TIW155Z

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

N480425005401 followed by a unit qualifier and the quantity

Package 80425-0054-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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 500 mg/1TabletOralBryant Ranch Prepack71335-1391
NabumetoneNabumetone 750 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-540
NabumetoneNabumetone 500 mg/1TabletOralRedpharm Drug67296-2137
NabumetoneNabumetone 500 mg/1TabletOralSportpharm LLC85766-261
NabumetoneNabumetone 750 mg/1TabletOralSportpharm LLC85766-262
NabumetoneNabumetone 500 mg/1TabletOralBryant Ranch Prepack63629-8508
NabumetoneNabumetone 500 mg/1TabletOralBryant Ranch Prepack63629-8506
NabumetoneNabumetone 500 mg/1TabletOralREMEDYREPACK INC.70518-3835
NabumetoneNabumetone 750 mg/1TabletOralBryant Ranch Prepack63629-8509
NabumetoneNabumetone 750 mg/1TabletOralBryant Ranch Prepack63629-8510
NabumetoneNabumetone 750 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-040
NabumetoneNabumetone 500 mg/1TabletOraldirect rx72189-184
NabumetoneNabumetone 500 mg/1TabletOralProficient Rx LP71205-977
NabumetoneNabumetone 750 mg/1TabletOralProficient Rx LP71205-978
NabumetoneNabumetone 750 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7597
NabumetoneNabumetone 750 mg/1TabletOralBryant Ranch Prepack71335-1559
NabumetoneNabumetone 750 mg/1TabletOralNorthwind Health Company, LLC51655-733
NabumetoneNabumetone 750 mg/1TabletOralREMEDYREPACK INC.70518-4047
NabumetoneNabumetone 500 mg/1TabletOralBryant Ranch Prepack72162-1557

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