NDC codes

FDA NDC Directory
Product NDC (as listed)68084-721Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68084-0721Add 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
68084-721-216808407212130 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-721-21) / 1 TABLET in 1 BLISTER PACK (68084-721-11)Marketed from Jun 2, 2014

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)
Modafinil
Generic name (nonproprietary)
modafinil
Active ingredients
Modafinil — 200 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202566
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
Identifiers
Product ID 68084-721_25c5e078-ef5a-651d-e063-6394a90a2845SPL ID 25c5e078-ef5a-651d-e063-6394a90a2845SPL set ID 928a3ab6-b53c-4924-882c-9f2f49aba0f1RxCUI 205324, 260218UNII R3UK8X3U3D
Pharmacologic class
Sympathomimetic-like Agent

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

N468084072121 followed by a unit qualifier and the quantity

Package 68084-0721-21. 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 202566

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

FDA NDC Directory listings under ANDA 202566
ProductStrengthForm · routeLabelerProduct NDC
ModafinilModafinil 100 mg/1TabletOralAurobindo Pharma Limited65862-601
ModafinilModafinil 200 mg/1TabletOralProficient Rx LP71205-544
ModafinilModafinil 200 mg/1TabletOralAurobindo Pharma Limited65862-602
ModafinilModafinil 200 mg/1TabletOralASCLEMED USA INC.87063-307
ModafinilModafinil 100 mg/1TabletOralASCLEMED USA INC.87063-306
ModafinilModafinil 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5121
ModafinilModafinil 100 mg/1TabletOralAvPAK50268-570
ModafinilModafinil 200 mg/1TabletOralAvPAK50268-571
ModafinilModafinil 100 mg/1TabletOralAmerican Health Packaging68084-621
ModafinilModafinil 100 mg/1TabletOralBryant Ranch Prepack71335-1122
ModafinilModafinil 100 mg/1TabletOralProficient Rx LP71205-477
ModafinilModafinil 200 mg/1TabletOralBryant Ranch Prepack71335-1173
ModafinilModafinil 200 mg/1TabletOralBryant Ranch Prepack63629-7315
ModafinilModafinil 100 mg/1TabletOralRising Pharma Holdings, Inc.57237-154
ModafinilModafinil 200 mg/1TabletOralRising Pharma Holdings, Inc.57237-155

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