Haloperidol NDC 82619-107

NDC codes

FDA NDC Directory

Product NDC (as listed)82619-107Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82619-0107Add 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 NDC	11-digit (billing)	Package	Copy
82619-107-01	82619010701	100 TABLET in 1 BOTTLE (82619-107-01)Marketed from Jan 5, 2026
82619-107-02	82619010702	1000 TABLET in 1 BOTTLE (82619-107-02)Marketed from Jan 5, 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 — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Creekwood Pharmaceuticals LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218162
Marketing start: Jan 5, 2026
Listing expires: Dec 31, 2026
Identifiers: Product ID 82619-107_46d58435-0437-e206-e063-6294a90ae755SPL ID 46d58435-0437-e206-e063-6294a90ae755SPL set ID 9763c044-7430-48f7-bf3e-da1c7c683955RxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3DUPC 0382619105018, 0382619105025, 0382619108033, 0382619109023, 0382619109016, 0382619109030, 0382619110029, 0382619106022, 0382619107029, 0382619106015, 0382619107012, 0382619108026
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

N482619010701 followed by a unit qualifier and the quantity

Package 82619-0107-01. 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
Product	Strength	Form · route	Labeler	Product NDC
Haloperidol	Haloperidol .5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2621
Haloperidol	Haloperidol 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2624
Haloperidol	Haloperidol 1 mg/1	TabletOral	Bryant Ranch Prepack	72162-2622
Haloperidol	Haloperidol 2 mg/1	TabletOral	Bryant Ranch Prepack	72162-2623
Haloperidol	Haloperidol 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2625
Haloperidol	Haloperidol 20 mg/1	TabletOral	Bryant Ranch Prepack	72162-2626
Haloperidol	Haloperidol 1 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-106
Haloperidol	Haloperidol .5 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-105
Haloperidol	Haloperidol 5 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-108
Haloperidol	Haloperidol 10 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-109
Haloperidol	Haloperidol 20 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-110