NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2626Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2626Add 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
72162-2626-172162262601100 TABLET in 1 BOTTLE (72162-2626-1)Marketed from Apr 21, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218162
Marketing start
Listing expires
Identifiers
Product ID 72162-2626_7ce2ea8a-01a8-4d19-b9ba-bd955728615aSPL ID 7ce2ea8a-01a8-4d19-b9ba-bd955728615aSPL set ID 7666e56f-9eef-4343-8a76-60613c4ca57fRxCUI 197754UNII J6292F8L3D
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

N472162262601 followed by a unit qualifier and the quantity

Package 72162-2626-01. 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 218162

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

FDA NDC Directory listings under ANDA 218162
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol .5 mg/1TabletOralBryant Ranch Prepack72162-2621
HaloperidolHaloperidol 5 mg/1TabletOralBryant Ranch Prepack72162-2624
HaloperidolHaloperidol 1 mg/1TabletOralBryant Ranch Prepack72162-2622
HaloperidolHaloperidol 2 mg/1TabletOralBryant Ranch Prepack72162-2623
HaloperidolHaloperidol 10 mg/1TabletOralBryant Ranch Prepack72162-2625
HaloperidolHaloperidol 1 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-106
HaloperidolHaloperidol .5 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-105
HaloperidolHaloperidol 5 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-108
HaloperidolHaloperidol 2 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-107
HaloperidolHaloperidol 10 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-109
HaloperidolHaloperidol 20 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-110

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