Nabumetone 1000 mg (nabumetone) NDC 79739-7078

NDC codes

FDA NDC Directory

Product NDC (as listed)79739-7078Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79739-7078Add 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
79739-7078-1	79739707801	100 TABLET, FILM COATED in 1 BOTTLE (79739-7078-1)Marketed from Sep 4, 2019
79739-7078-3	79739707803	30 TABLET, FILM COATED in 1 BOTTLE (79739-7078-3)Marketed from Oct 2, 2019
79739-7078-6	79739707806	60 TABLET, FILM COATED in 1 BOTTLE (79739-7078-6)Marketed from Jul 24, 2020

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 1000 mg
Generic name (nonproprietary): nabumetone
Active ingredients: Nabumetone — 1000 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: LGM PHARMA SOLUTIONS, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203166
Marketing start: Sep 4, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 79739-7078_cf52d275-4853-4576-832a-07630bb644dcSPL ID cf52d275-4853-4576-832a-07630bb644dcSPL set ID ef7c3da8-797f-4ea9-8999-53509785a0f7RxCUI 311892, 311893, 427726UNII LW0TIW155Z
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

N479739707801 followed by a unit qualifier and the quantity

Package 79739-7078-01. 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 203166

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

FDA NDC Directory listings under ANDA 203166
Product	Strength	Form · route	Labeler	Product NDC
Relafen Dsnabumetone	Nabumetone 1000 mg/1	TabletOral	Carwin Pharmaceutical Associates, LLC	15370-170
Nabumetone 500 mgnabumetone	Nabumetone 500 mg/1	Tablet, Film coatedOral	LGM PHARMA SOLUTIONS, LLC	79739-7076
Nabumetone 750 mgnabumetone	Nabumetone 750 mg/1	Tablet, Film coatedOral	LGM PHARMA SOLUTIONS, LLC	79739-7077