NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4725Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4725Add 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
70518-4725-07051847250070518472500100 POUCH in 1 BOX (70518-4725-0) / 1 TABLET in 1 POUCH (70518-4725-1)Marketed from Aug 12, 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 — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216918
Marketing start
Listing expires
Identifiers
Product ID 70518-4725_590115aa-2728-b742-e063-6394a90aa6afSPL ID 590115aa-2728-b742-e063-6394a90aa6afSPL set ID addb5b30-d1f8-47dd-ba4c-94d0b01ae17cRxCUI 314035UNII 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

N470518472500 followed by a unit qualifier and the quantity

Package 70518-4725-00. 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)

About NDC 70518-4725

What is NDC 70518-4725?
70518-4725 is the product NDC for Haloperidol, Haloperidol 10 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, 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?
REMEDYREPACK INC., NDC labeler code 70518. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
HaloperidolHaloperidol .5 mg/1TabletOralAjanta Pharma USA Inc.27241-26427241-0264-01
HaloperidolHaloperidol 1 mg/1TabletOralAjanta Pharma USA Inc.27241-26527241-0265-01
HaloperidolHaloperidol 2 mg/1TabletOralAjanta Pharma USA Inc.27241-26627241-0266-01
HaloperidolHaloperidol 5 mg/1TabletOralAjanta Pharma USA Inc.27241-26727241-0267-01
HaloperidolHaloperidol 10 mg/1TabletOralAjanta Pharma USA Inc.27241-26827241-0268-01
HaloperidolHaloperidol 20 mg/1TabletOralAjanta Pharma USA Inc.27241-26927241-0269-01
HaloperidolHaloperidol 5 mg/1TabletOralCoupler LLC67046-032967046-0329-03
HaloperidolHaloperidol 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-03787441-0037-01
HaloperidolHaloperidol .5 mg/1TabletOralSafecor Health, LLC48433-15148433-0151-20
HaloperidolHaloperidol 1 mg/1TabletOralSafecor Health, LLC48433-15248433-0152-20

All 171 Haloperidol NDCs

Other NDCs under ANDA 216918

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

FDA NDC Directory listings under ANDA 216918
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8626
HaloperidolHaloperidol 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8627
HaloperidolHaloperidol .5 mg/1TabletOralLifestar Pharma LLC70756-001
HaloperidolHaloperidol 5 mg/1TabletOralREMEDYREPACK INC.70518-4285
HaloperidolHaloperidol 1 mg/1TabletOralLifestar Pharma LLC70756-002
HaloperidolHaloperidol 2 mg/1TabletOralLifestar Pharma LLC70756-003
HaloperidolHaloperidol 5 mg/1TabletOralLifestar Pharma LLC70756-004
HaloperidolHaloperidol 2 mg/1TabletOralMajor Pharmaceuticals0904-7504
HaloperidolHaloperidol 20 mg/1TabletOralLifestar Pharma LLC70756-236
HaloperidolHaloperidol 10 mg/1TabletOralLifestar Pharma LLC70756-242

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