What is NDC 69339-179?

69339-179 is the product NDC for Armodafinil, Armodafinil 200 mg/1 tablet, listed with the FDA by Natco Pharma USA LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Natco Pharma USA LLC, NDC labeler code 69339. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Armodafinil?

27 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Armodafinil NDC 69339-179 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69339-179Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69339-0179Add 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
69339-179-03	6933901790369339017903	30 TABLET in 1 BOTTLE (69339-179-03)Marketed from Mar 23, 2023
69339-179-10	6933901791069339017910	1000 TABLET in 1 BOTTLE (69339-179-10)Marketed from Mar 23, 2023

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): Armodafinil
Generic name (nonproprietary): armodafinil
Active ingredients: Armodafinil — 200 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Natco Pharma USA LLCNDC labeler code 69339
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202768
Marketing start: Mar 23, 2023
Listing expires: Dec 31, 2027
DEA schedule: CIV
Identifiers: Product ID 69339-179_d93dca81-a0da-49ee-be61-86e713ab56cdSPL ID d93dca81-a0da-49ee-be61-86e713ab56cdSPL set ID de2f0921-e791-426c-9192-2b7162e2158cRxCUI 724859, 724861, 724863, 861960UNII V63XWA605IUPC 0369339177105, 0369339180051, 0369339178102, 0369339178034, 0369339180037, 0369339179031

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

N469339017903 followed by a unit qualifier and the quantity

Package 69339-0179-03. 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 Dec 5, 2023.

Indications (excerpt from the label)

Armodafinil tablets are indicated to improve wakefulness in adult patients with excessive sleepiness associated with obstructive sleep apnea (OSA), narcolepsy, or shift work disorder (SWD). Limitations of Use In OSA, armodafinil tablets are indicated to treat excessive sleepiness and not as treatment for the underlying obstruction. If continuous positive airway pressure (CPAP) is the treatment of choice for a patient, a maximal effort to treat with CPAP for an adequate period of time should be made prior to initiating armodafinil tablets for excessive sleepiness. Armodafinil tablets are indicated to improve wakefulness in adult patients with excessive sleepiness associated with obstructive s…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69339-179

What is NDC 69339-179?: 69339-179 is the product NDC for Armodafinil, Armodafinil 200 mg/1 tablet, listed with the FDA by Natco Pharma USA LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Armodafinil.
What is the active ingredient?: Armodafinil.
Who is the labeler?: Natco Pharma USA LLC, NDC labeler code 69339. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Armodafinil?: 27 other product NDCs are listed under this name. See all Armodafinil 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 Armodafinil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Armodafinil	Armodafinil 50 mg/1	TabletOral	Direct_Rx	72189-464	72189-0464-30
Armodafinil	Armodafinil 50 mg/1	TabletOral	Natco Pharma USA LLC	69339-177	69339-0177-0369339-0177-10
Armodafinil	Armodafinil 150 mg/1	TabletOral	Natco Pharma USA LLC	69339-178	69339-0178-0369339-0178-10
Armodafinil	Armodafinil 250 mg/1	TabletOral	Natco Pharma USA LLC	69339-180	69339-0180-0369339-0180-05
Armodafinil	Armodafinil 200 mg/1	TabletOral	DirectRx	72189-353	72189-0353-30
Armodafinil	Armodafinil 250 mg/1	TabletOral	direct rx	72189-261	72189-0261-30
Armodafinil	Armodafinil 150 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7880	68788-7880-0368788-7880-0668788-7880-09
Armodafinil	Armodafinil 200 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7826	68788-7826-0368788-7826-0668788-7826-09
Armodafinil	Armodafinil 250 mg/1	TabletOral	direct rx	72189-133	72189-0133-30
Armodafinil	Armodafinil 200 mg/1	TabletOral	Aurobindo Pharma Limited	65862-998	65862-0998-30

All 28 Armodafinil NDCs

Other NDCs under ANDA 202768

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

FDA NDC Directory listings under ANDA 202768
Product	Strength	Form · route	Labeler	Product NDC
Armodafinil	Armodafinil 50 mg/1	TabletOral	Natco Pharma USA LLC	69339-177
Armodafinil	Armodafinil 150 mg/1	TabletOral	Natco Pharma USA LLC	69339-178
Armodafinil	Armodafinil 250 mg/1	TabletOral	Natco Pharma USA LLC	69339-180