NDC codes

FDA NDC Directory
Product NDC (as listed)70756-242Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70756-0242Add 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
70756-242-1170756024211100 TABLET in 1 BOTTLE (70756-242-11)Marketed from Apr 11, 2024
70756-242-12707560242121000 TABLET in 1 BOTTLE (70756-242-12)Marketed from Apr 11, 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 — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216918
Marketing start
Listing expires
Identifiers
Product ID 70756-242_7b545974-2d39-4106-8975-76c124a6c5eeSPL ID 7b545974-2d39-4106-8975-76c124a6c5eeSPL set ID 00bb61c8-db35-4c04-9ef7-47d447d2496bRxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3DUPC 0370756242123, 0370756003120, 0370756004127, 0370756236122
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

N470756024211 followed by a unit qualifier and the quantity

Package 70756-0242-11. 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 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 1 mg/1TabletOralLifestar Pharma LLC70756-002
HaloperidolHaloperidol .5 mg/1TabletOralLifestar Pharma LLC70756-001
HaloperidolHaloperidol 2 mg/1TabletOralLifestar Pharma LLC70756-003
HaloperidolHaloperidol 5 mg/1TabletOralLifestar Pharma LLC70756-004
HaloperidolHaloperidol 10 mg/1TabletOralREMEDYREPACK INC.70518-4725
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/1TabletOralREMEDYREPACK INC.70518-4285
HaloperidolHaloperidol 20 mg/1TabletOralLifestar Pharma LLC70756-236
HaloperidolHaloperidol 2 mg/1TabletOralMajor Pharmaceuticals0904-7504

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Haloperidol NDC 70756-242 | Med-Code