NDC codes

FDA NDC Directory
Product NDC (as listed)0378-0257Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00378-0257Add 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
0378-0257-10003780257101000 TABLET in 1 BOTTLE, PLASTIC (0378-0257-10)Marketed from Jun 10, 1986

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 1 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070278
Marketing start
Marketing end
Identifiers
Product ID 0378-0257_1b33ae94-4fa5-4298-a713-3e049c47588cSPL ID 1b33ae94-4fa5-4298-a713-3e049c47588cSPL set ID c559b0b0-4087-d12a-e718-c18ccb6811e6RxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3DUPC 0303780351011
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

N400378025710 followed by a unit qualifier and the quantity

Package 00378-0257-10. 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 070278

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

FDA NDC Directory listings under ANDA 070278
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol 1 mg/1TabletOralMylan Institutional Inc.51079-734
HaloperidolHaloperidol .5 mg/1TabletOralMylan Institutional Inc.51079-733
HaloperidolHaloperidol 2 mg/1TabletOralMylan Institutional Inc.51079-735
HaloperidolHaloperidol 5 mg/1TabletOralMylan Institutional Inc.51079-736
HaloperidolHaloperidol 2 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0214
HaloperidolHaloperidol .5 mg/1TabletOralCoupler LLC67046-1496
HaloperidolHaloperidol 5 mg/1TabletOralCardinal Health 107, LLC55154-5059
HaloperidolHaloperidol 5 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0327
HaloperidolHaloperidol .5 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0351

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Haloperidol NDC 0378-0257 | Med-Code