NDC codes

FDA NDC Directory
Product NDC (as listed)0378-3432Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00378-3432Add 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
0378-3432-93003783432930037834329330 TABLET in 1 BOTTLE, PLASTIC (0378-3432-93)Marketed from Jun 1, 2016

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 150 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Mylan Pharmaceuticals Inc.NDC labeler code 0378
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200043
Marketing start
Listing expires
DEA schedule
CIV
Identifiers
Product ID 0378-3432_34fcca9f-37ba-40d9-9032-6ffeeb031a36SPL ID 34fcca9f-37ba-40d9-9032-6ffeeb031a36SPL set ID de0799f7-7644-4057-a7da-75436f978c61RxCUI 724859, 724861, 724863UNII V63XWA605IUPC 0303783433936, 0303783431932, 0303783432939

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

N400378343293 followed by a unit qualifier and the quantity

Package 00378-3432-93. 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 .

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 0378-3432

What is NDC 0378-3432?
0378-3432 is the product NDC for Armodafinil, Armodafinil 150 mg/1 tablet, listed with the FDA by Mylan Pharmaceuticals Inc.. It has 1 package NDC, 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?
Mylan Pharmaceuticals Inc., NDC labeler code 0378. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ArmodafinilArmodafinil 50 mg/1TabletOralDirect_Rx72189-46472189-0464-30
ArmodafinilArmodafinil 50 mg/1TabletOralNatco Pharma USA LLC69339-17769339-0177-0369339-0177-10
ArmodafinilArmodafinil 150 mg/1TabletOralNatco Pharma USA LLC69339-17869339-0178-0369339-0178-10
ArmodafinilArmodafinil 200 mg/1TabletOralNatco Pharma USA LLC69339-17969339-0179-0369339-0179-10
ArmodafinilArmodafinil 250 mg/1TabletOralNatco Pharma USA LLC69339-18069339-0180-0369339-0180-05
ArmodafinilArmodafinil 200 mg/1TabletOralDirectRx72189-35372189-0353-30
ArmodafinilArmodafinil 250 mg/1TabletOraldirect rx72189-26172189-0261-30
ArmodafinilArmodafinil 150 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-788068788-7880-0368788-7880-0668788-7880-09
ArmodafinilArmodafinil 200 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-782668788-7826-0368788-7826-0668788-7826-09
ArmodafinilArmodafinil 250 mg/1TabletOraldirect rx72189-13372189-0133-30

All 28 Armodafinil NDCs

Other NDCs under ANDA 200043

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

FDA NDC Directory listings under ANDA 200043
ProductStrengthForm · routeLabelerProduct NDC
ArmodafinilArmodafinil 50 mg/1TabletOralMylan Pharmaceuticals Inc.0378-3431
ArmodafinilArmodafinil 250 mg/1TabletOralMylan Pharmaceuticals Inc.0378-3433
ArmodafinilArmodafinil 150 mg/1TabletOralBryant Ranch Prepack71335-2991

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