NDC codes

FDA NDC Directory
Product NDC (as listed)68382-409Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68382-0409Add 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
68382-409-0168382040901100 TABLET in 1 BOTTLE (68382-409-01)Marketed from Feb 1, 2023
68382-409-10683820409101000 TABLET in 1 BOTTLE (68382-409-10)Marketed from Feb 1, 2023
68382-409-776838204097710 BLISTER PACK in 1 CARTON (68382-409-77) / 10 TABLET in 1 BLISTER PACK (68382-409-30)Marketed from Feb 1, 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)
Haloperidol
Generic name (nonproprietary)
haloperidol
Active ingredients
Haloperidol — 2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077580
Marketing start
Listing expires
Identifiers
Product ID 68382-409_8d46c061-97af-4b2c-a788-bb08031d2c6fSPL ID 8d46c061-97af-4b2c-a788-bb08031d2c6fSPL set ID 54502f78-7244-454a-9171-4e73127f1456RxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3DUPC 0368382409010, 0368382080011, 0368382408013
Pharmacologic class
Typical Antipsychotic

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

N468382040901 followed by a unit qualifier and the quantity

Package 68382-0409-01. 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 077580

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

FDA NDC Directory listings under ANDA 077580
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol 5 mg/1TabletOralMajor Pharmaceuticals0904-6782
HaloperidolHaloperidol 1 mg/1TabletOralCoupler LLC67046-1255
HaloperidolHaloperidol .5 mg/1TabletOralSafecor Health, LLC48433-151
HaloperidolHaloperidol 5 mg/1TabletOralZydus Lifesciences Limited65841-626
HaloperidolHaloperidol 1 mg/1TabletOralSafecor Health, LLC48433-152
HaloperidolHaloperidol 10 mg/1TabletOralZydus Lifesciences Limited65841-627
HaloperidolHaloperidol .5 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-407
HaloperidolHaloperidol 2 mg/1TabletOralSafecor Health, LLC48433-153
HaloperidolHaloperidol 20 mg/1TabletOralZydus Lifesciences Limited65841-628
HaloperidolHaloperidol 1 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-408
HaloperidolHaloperidol 10 mg/1TabletOralAmerican Health Packaging68084-249
HaloperidolHaloperidol 20 mg/1TabletOralAmerican Health Packaging68084-250
HaloperidolHaloperidol 5 mg/1TabletOralCoupler LLC67046-0329
HaloperidolHaloperidol 5 mg/1TabletOralCardinal Health 107, LLC55154-3566
HaloperidolHaloperidol 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-037
HaloperidolHaloperidol 2 mg/1TabletOralZydus Lifesciences Limited65841-839
HaloperidolHaloperidol 20 mg/1TabletOralCoupler LLC67046-1544
HaloperidolHaloperidol .5 mg/1TabletOralZydus Lifesciences Limited65841-837
HaloperidolHaloperidol 10 mg/1TabletOralMajor Pharmaceuticals0904-6733
HaloperidolHaloperidol 1 mg/1TabletOralZydus Lifesciences Limited65841-838

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