What is NDC 72888-173?

72888-173 is the product NDC for Haloperidol, Haloperidol 2 mg/mL solution, concentrate, listed with the FDA by Advagen Pharma Ltd. It has 2 package NDCs, shown above in 10- and 11-digit form.

Advagen Pharma Ltd, NDC labeler code 72888. 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 72888-173 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72888-173Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72888-0173Add 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
72888-173-47	7288801734772888017347	15 mL in 1 BOTTLE (72888-173-47)Marketed from Jan 31, 2024
72888-173-48	7288801734872888017348	120 mL in 1 BOTTLE (72888-173-48)Marketed from Jan 31, 2024

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/mL
Dosage form: Solution, Concentrate
Route: Oral
Labeler: Advagen Pharma LtdNDC labeler code 72888
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218371
Marketing start: Jan 31, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 72888-173_45c7bbb4-7235-89a8-e063-6394a90a7ea0SPL ID 45c7bbb4-7235-89a8-e063-6394a90a7ea0SPL set ID 8bfdc739-51b4-4914-9a60-923e83762307RxCUI 141935UNII J6292F8L3DUPC 0372888173474, 0372888173481
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

N472888017347 followed by a unit qualifier and the quantity

Package 72888-0173-47. 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 12, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Haloperidol oral solution is indicated for use in the management of manifestations of psychotic disorders. Haloperidol oral solution is indicated for the control of tics and vocal utterances of Tourette's Disorder in children and adults. Haloperidol oral solution is effective for the treatment of severe behavior problems in children of combative, explosive hyperexcitability (which cannot be accounted for by immediate provocation). Haloperidol is 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 att…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72888-173

What is NDC 72888-173?: 72888-173 is the product NDC for Haloperidol, Haloperidol 2 mg/mL solution, concentrate, listed with the FDA by Advagen Pharma Ltd. 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?: Advagen Pharma Ltd, NDC labeler code 72888. 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