NDC codes

FDA NDC Directory
Product NDC (as listed)87063-308Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87063-0308Add 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
87063-308-018706303080187063030801100 TABLET in 1 BOTTLE (87063-308-01)Marketed from Sep 10, 2026
87063-308-30870630308308706303083030 TABLET in 1 BOTTLE (87063-308-30)Marketed from Sep 10, 2026
87063-308-60870630308608706303086060 TABLET in 1 BOTTLE (87063-308-60)Marketed from Sep 10, 2026
87063-308-90870630308908706303089090 TABLET in 1 BOTTLE (87063-308-90)Marketed from Sep 10, 2026

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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
ASCLEMED USA INC.NDC labeler code 87063
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209966
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
Identifiers
Product ID 87063-308_5b1b1793-3c64-3f34-e063-6294a90aa7abSPL ID 5b1b1793-3c64-3f34-e063-6294a90aa7ab
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

N487063030801 followed by a unit qualifier and the quantity

Package 87063-0308-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 87063-308

What is NDC 87063-308?
87063-308 is the product NDC for Modafinil, Modafinil 100 mg/1 tablet, listed with the FDA by ASCLEMED USA INC.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Modafinil.
What is the active ingredient?
Modafinil.
Who is the labeler?
ASCLEMED USA INC., NDC labeler code 87063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Modafinil?
49 other product NDCs are listed under this name. See all Modafinil 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 Modafinil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ModafinilModafinil 200 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-865368788-8653-0368788-8653-0668788-8653-09
ModafinilModafinil 200 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-86223155-0862-0123155-0862-0323155-0862-05+1 more
ModafinilModafinil 200 mg/1TabletOralBryant Ranch Prepack71335-250171335-2501-0071335-2501-0171335-2501-02+7 more
ModafinilModafinil 200 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-828068788-8280-0368788-8280-0668788-8280-09
ModafinilModafinil 100 mg/1TabletOralBionpharma Inc.69452-34269452-0342-1369452-0342-1969452-0342-20
ModafinilModafinil 200 mg/1TabletOralBionpharma Inc.69452-34369452-0343-1369452-0343-1969452-0343-20
ModafinilModafinil 200 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-98971610-0989-3071610-0989-5371610-0989-60
ModafinilModafinil 100 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-60423155-0604-0123155-0604-0323155-0604-05+1 more
ModafinilModafinil 200 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-60523155-0605-0123155-0605-0323155-0605-05+1 more
ModafinilModafinil 200 mg/1TabletOralBryant Ranch Prepack71335-225871335-2258-0071335-2258-0171335-2258-02+7 more

All 50 Modafinil NDCs

Other NDCs under ANDA 209966

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

FDA NDC Directory listings under ANDA 209966
ProductStrengthForm · routeLabelerProduct NDC
ModafinilModafinil 100 mg/1TabletOralGolden State Medical Supply, Inc.51407-960
ModafinilModafinil 200 mg/1TabletOralGolden State Medical Supply, Inc.51407-961
ModafinilModafinil 100 mg/1TabletOralZydus Lifesciences Limited70771-1051
ModafinilModafinil 200 mg/1TabletOralZydus Lifesciences Limited70771-1052
ModafinilModafinil 200 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-873
ModafinilModafinil 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-976
ModafinilModafinil 200 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-991
ModafinilModafinil 100 mg/1TabletOralViona Pharmaceuticals Inc72578-005
ModafinilModafinil 200 mg/1TabletOralViona Pharmaceuticals Inc72578-006
ModafinilModafinil 200 mg/1TabletOralProficient Rx LP82804-126
ModafinilModafinil 200 mg/1TabletOralASCLEMED USA INC.87063-309

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