What is NDC 82619-107?

82619-107 is the product NDC for Haloperidol, Haloperidol 2 mg/1 tablet, listed with the FDA by Creekwood Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Creekwood Pharmaceuticals LLC, NDC labeler code 82619. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Haloperidol?

170 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Haloperidol NDC 82619-107 | National Drug Code

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	8261901070182619010701	100 TABLET in 1 BOTTLE (82619-107-01)Marketed from Jan 5, 2026
82619-107-02	8261901070282619010702	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 LLCNDC labeler code 82619
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

Current FDA label (SPL), effective Dec 26, 2025. 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)

About NDC 82619-107

What is NDC 82619-107?: 82619-107 is the product NDC for Haloperidol, Haloperidol 2 mg/1 tablet, listed with the FDA by Creekwood Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Haloperidol.
What is the active ingredient?: Haloperidol.
Who is the labeler?: Creekwood Pharmaceuticals LLC, NDC labeler code 82619. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Haloperidol?: 170 other product NDCs are listed under this name. See all Haloperidol 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 Haloperidol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Haloperidol	Haloperidol .5 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-264	27241-0264-01
Haloperidol	Haloperidol 1 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-265	27241-0265-01
Haloperidol	Haloperidol 2 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-266	27241-0266-01
Haloperidol	Haloperidol 5 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-267	27241-0267-01
Haloperidol	Haloperidol 10 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-268	27241-0268-01
Haloperidol	Haloperidol 20 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-269	27241-0269-01
Haloperidol	Haloperidol 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4725	70518-4725-00
Haloperidol	Haloperidol 5 mg/1	TabletOral	Coupler LLC	67046-0329	67046-0329-03
Haloperidol	Haloperidol 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-037	87441-0037-01
Haloperidol	Haloperidol .5 mg/1	TabletOral	Safecor Health, LLC	48433-151	48433-0151-20

All 171 Haloperidol NDCs

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 1 mg/1	TabletOral	Bryant Ranch Prepack	72162-2622
Haloperidol	Haloperidol 2 mg/1	TabletOral	Bryant Ranch Prepack	72162-2623
Haloperidol	Haloperidol 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2624
Haloperidol	Haloperidol 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2625
Haloperidol	Haloperidol 20 mg/1	TabletOral	Bryant Ranch Prepack	72162-2626
Haloperidol	Haloperidol .5 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-105
Haloperidol	Haloperidol 1 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-106
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