NDC codes

FDA NDC Directory
Product NDC (as listed)72789-559Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0559Add 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
72789-559-0172789055901100 TABLET in 1 BOTTLE, PLASTIC (72789-559-01)Marketed from Apr 22, 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)
Haloperidol
Generic name (nonproprietary)
haloperidol
Active ingredients
Haloperidol — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071130
Marketing start
Listing expires
Identifiers
Product ID 72789-559_50221596-087a-9973-e063-6394a90ae95fSPL ID 50221596-087a-9973-e063-6394a90ae95fSPL set ID 533b0b4c-cbd6-4ec0-a333-8b04b5b43a1dRxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3DUPC 0372789566016, 0372789559018, 0372789569017, 0372789568010, 0372789558011, 0372789567013
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

N472789055901 followed by a unit qualifier and the quantity

Package 72789-0559-01. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Haloperidol tablets are indicated for use in the management of manifestations of psychotic disorders. Haloperidol tablets are indicated for the control of tics and vocal utterances of Tourette’s Disorder in children and adults. Haloperidol tablets are effective for the treatment of severe behavior problems in children of combative, explosive hyperexcitability (which cannot be accounted for by immediate provocation). Haloperidol tablets are also effective in the short-term treatment of hyperactive children who show excessive motor activity with accompanying conduct disorders consisting of some or all of the following symptoms: impulsivity, difficulty sustaining attention…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 071130

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

FDA NDC Directory listings under ANDA 071130
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-558
HaloperidolHaloperidol .5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-566
HaloperidolHaloperidol 1 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-567
HaloperidolHaloperidol 2 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-568
HaloperidolHaloperidol 20 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-569
HaloperidolHaloperidol 2 mg/1TabletOralAiPing Pharmaceutical, Inc11788-073
HaloperidolHaloperidol .5 mg/1TabletOralAiPing Pharmaceutical, Inc11788-071
HaloperidolHaloperidol 1 mg/1TabletOralAiPing Pharmaceutical, Inc11788-072
HaloperidolHaloperidol 20 mg/1TabletOralAiPing Pharmaceutical, Inc11788-076
HaloperidolHaloperidol 5 mg/1TabletOralAiPing Pharmaceutical, Inc11788-074
HaloperidolHaloperidol 10 mg/1TabletOralAiPing Pharmaceutical, Inc11788-075

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Haloperidol NDC 72789-559 | Med-Code